Immunostimulatory compositions

ABSTRACT

The present disclosure relates to immunostimulatory compositions that are effective in eliciting immune responses in avian species. More specifically, these immunostimulatory compositions comprise an immunomodulator composition and an immunostimulatory oligonucleotide that when administered stimulate toll-like receptor 21.

REFERENCE TO RELATED APPLICATIONS

This application claims priority to and the benefit of European Patent Application Nos. EP17207740.6, EP17207746.3, and EP17207750.5, each filed Dec. 15, 2017, the disclosures of which are incorporated herein by reference in their entireties.

SEQUENCE LISTING

This application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created Nov. 30, 2018, is named BHC_168027_SL.txt and is 92,167 bytes in size.

FIELD OF THE INVENTION

Compositions and methods for stimulating toll-like receptor protein 21 (TLR21) are provided. More specifically, immunostimulatory oligonucleotides and compositions, methods of making immunostimulatory oligonucleotides and compositions, and methods of stimulating TLR21 are disclosed herein.

BACKGROUND OF THE INVENTION

The immune systems of vertebrates have evolved molecular mechanisms for recognizing invading pathogens and initiating cellular signaling pathways to actively resist infection. Some of the molecular mechanisms are specific for a particular microbe and involve biomolecules such as antibodies that recognize the surface antigens of a single species of pathogen. Unfortunately, pathogen-specific defense mechanisms are not completely effective as some animals do not develop any acquired resistance until after infection has set in, and in some instances, the pathogen has evolved stealthy means for evading a vertebrate's acquired defenses.

Vertebrates also recognize infections more generally, and this recognition leads to non-specific immune responses such as an uptick in cytokine expression. This defense can be elicited when cellular receptors bind to pathogen-associated molecular patterns (PAMPs). This interaction between the PAMP and the host's cognate receptor for the PAMP can initiate an immune response. For example, toll-like receptor protein 21 (TLR21) is the chicken functional homolog of mammalian TLR9 and is capable of recognizing unmethylated CpG motifs, which have a higher CpG content in microbes than in vertebrates. Known methodologies leverage this nonspecific immune response pathway by administering plasmids or oligonucleotides having unmethylated CpG motifs, and activation of TLR21 by CpG motif-containing nucleic acids has been shown to activate cellular signals involved in the immune responses to microbial infections. However, administered immunostimulatory plasmids or oligonucleotides alone may fail to elicit a response sufficient to combat infection.

Large-scale animal producers are in dire need of alternatives to antibiotic treatment of infections. Consumers are pressing these producers for antibiotic-free animal products, and at the same time, increasing incidence of infection due to antibiotic resistant pathogens is illuminating the dangers of administering antibiotics prophylactically to large populations. Similarly, antibiotic resistance is becoming a national emergency in human healthcare. Hospitals and doctors' office are becoming ground zero for the emergence of drug resistance bacteria such as multiple resistance Staphylococcus aureus (MRSA).

Thus, there is a need for immunostimulatory compositions and methods for eliciting non-specific immune responses against pathogens. The disclosed methods and compositions are directed to these and other important needs.

SUMMARY OF THE INVENTION

Disclosed herein are immunostimulatory compositions comprising an immunomodulator composition comprising a nucleic acid plasmid and a liposomal delivery vehicle; and an immunostimulatory oligonucleotide having at least one CpG motif and a guanine nucleotide-enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide

Also disclosed herein are methods for preparing an immunostimulatory composition comprising combining an immunomodulator composition comprising a nucleic acid plasmid and an immunostimulatory oligonucleotide to form an immunostimulatory composition, centrifuging the immunostimulatory composition to generate a supernatant and a pellet; and isolating the pellet.

Further provided are methods of stimulating TLR21 comprising administering an immunostimulatory oligonucleotide and an immunomodulator composition to a subject, wherein the immunostimulatory oligonucleotide comprises at least one CpG motif and a guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide, and wherein the immunomodulator composition comprises a noncoding nucleic acid plasmid and a cationic lipid delivery vehicle.

Methods are also disclosed for eliciting an immune response in a subject by administering an immunostimulatory oligonucleotide and an immunomodulator composition, or an immunostimulatory composition comprising an immunostimulatory oligonucleotide and an immunomodulator composition, to a subject, wherein the immunostimulatory oligonucleotide has at least one CpG motif and a guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide, and wherein the immunomodulator composition comprises a noncoding nucleic acid plasmid and a cationic lipid delivery vehicle

BRIEF DESCRIPTION OF THE DRAWINGS

The summary, as well as the following detailed description, is further understood when read in conjunction with the appended drawings. For the purpose of illustrating the disclosed compositions and methods, there are shown in the drawings exemplary embodiments of the compositions and methods; however, the compositions and methods are not limited to the specific embodiments disclosed. In the drawings:

FIG. 1 illustrates the chemical structure of a cholesteryl moiety attached to a tetraethylene glycol linker.

FIGS. 2A and 2B compare the immunogenicities of immunostimulatory plasmid DNA, plasmid DNA complexed with cationic liposomes, and immunostimulatory oligonucleotides. FIG. 2A compares the immunogenicities of an immunostimulatory plasmid DNA (“pDNA”) and pDNA complexed with cationic liposomes (“pDNA-F”). FIG. 2B compares the immunogenicities of pDNA, pDNA-F, and immunostimulatory oligonucleotide GCGT3-TG4T having a 5′-cholesteryl modification (“5Chol-GCGT3-TG4T”).

FIGS. 3A and 3B compare the immunogenicities of immunostimulatory plasmid DNA, immunostimulatory plasmid DNA complexed with cationic liposomes, immunostimulatory oligonucleotides, and combinations thereof. FIG. 3A compares the immunogenicities of pDNA, pDNA-F, 5Chol-GCGT3-TG4T, pDNA combined with 5′Chol-GCGT3-TG4T (“pDNA-5Chol-GCGT3-TG4T”), and pDNA-F combined with 5Chol-GCGT3-TG4T (“pDNA-F-5Chol-GCGT3-TG4T”), wherein the immunostimulatory oligonucleotides are at nM concentrations and pDNA and pDNA-F are at μg/ml concentrations. FIG. 3B depicts the differences in immunogenicity between pDNA, pDNA-F, 5Chol-GCGT3-TG4T, pDNA combined with 5′Chol-GCGT3-TG4T (“pDNA-5Chol-GCGT3-TG4T”), and pDNA-F combined with 5Chol-GCGT3-TG4T (“pDNA-F-5Chol-GCGT3-TG4T”), wherein the immunostimulatory oligonucleotides are at pM concentrations and pDNA and pDNA-F are at ng/ml concentrations;

FIG. 4 illustrates the ability of pDNA-F fractions to stimulate TLR21-mediated immune responses in HEK293-bsd-cTLR21 cells. Specifically, the immunogenicity of pDNA-F stored at 4° C. was compared to that of pDNA-F obtained in the pellet (“pDNA-F pellet”) and the supernatant (“pDNA-F supernatant”) of a centrifuged sample.

FIGS. 5A and 5B graphically depict the ability to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells of pDNA-F-5Chol-GCGT3-TG4T and 5Chol-GCGT3-TG4T at high and low concentrations, respectively.

FIGS. 6A and 6B compare the ability of high and low concentrations, respectively, of pDNA-F-5Chol-GCGT3-TG4T to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of 5Chol-GCGT3-TG4T obtained in the pellet (“pDNA-F 5Chol pellet”) and supernatant (“pDNA-F 5Chol Uberstand”) of a centrifuged pDNA-F sample.

FIGS. 7A and 7B compare the ability of high and low concentrations, respectively, of 5Chol-GCGT3-TG4T to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of 5Chol-GCGT3-TG4T obtained in the pellet (“5Chol pellet”) and supernatant (“5Chol Uberstand”) of a centrifuged pDNA-F sample.

FIGS. 8A and 8B compare the ability of high and low concentrations, respectively, of 5Chol-GCGT3-TG4T (“5Chol-GCGT3-TG4T 4° C.”) to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of pDNA-F combined with 5Chol-GCGT3-TG4T “pDNA-F/5-Chol-GCGT3-TG4T”).

FIGS. 9A and 9B compare the ability of high and low concentrations, respectively, of pDNA-F combined with 5Chol-GCGT3-TG4T (“pDNA-F/5-Chol-GCGT3-TG4T”) to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of pDNA-F combined with 5Chol-GCGT3-TG4T obtained in the pellet (“pDNA-F/5-Chol-GCGT3-TG4T pellet”) and supernatant (“pDNA-F/5-Chol-GCGT3-TG4T supernatant”) of a centrifuged pDNA-F sample.

FIGS. 10A and 10B compare the ability of high and low concentrations, respectively, of pDNA-F combined with 5Chol-GCGT3-TG4T (“pDNA-F-5-Chol-GCGT3-TG4T”) to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of pDNA-F and immunostimulatory oligonucleotide 5-Chol-GCGT3-TG4T.

FIGS. 11A and 11B compare the ability of high and low concentrations, respectively, of pDNA-F combined with 5Chol-GCGT3-TG4T (“pDNA-F-5-Chol-GCGT3-TG4T”) to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of pDNA-F combined with 5Chol-GCGT3-TG4T obtained in the pellet (“pDNA-F-5-Chol-GCGT3-TG4T pellet”) and supernatant (“pDNA-F-5-Chol-GCGT3-TG4T”) of a centrifuged pDNA-F sample.

FIGS. 12A and 12B compare the ability of high and low concentrations, respectively, of pDNA-F, immunostimulatory oligonucleotide GCGT3-TG4T, and pDNA-F complexed with GCGT3-TG4T (“pDNA-F-GCGT3-TG4T”) to generate TLR21-mediated immune responses in HEK293-bsd-cTLR21 cells.

FIGS. 13A and 13B compare the ability of high and low concentrations, respectively, of pDNA-F combined with immunostimulatory oligonucleotide GCGT3-TG4T (“pDNA-F-GCGT3-TG4T”) to generate a TLR21-mediated immune response in HEK293-bsd-cTLR21 cells to that of pDNA-F combined with immunostimulatory oligonucleotide GCGT3-TG4T obtained in the pellet (“pDNA-F-GCGT3-TG4T pellet”) and supernatant (“pDNA-F-GCGT3-TG4T supernatant”) of a centrifuged pDNA-F sample.

FIG. 14 depicts mean Haemagglutination inhibition (HI) titres (Log 2) (with standard deviation) results for ODN1 (GCGT3-TG4T-5Chol) at days 14 (top panel) and 21 (bottom panel) post vaccination (pv). Asterisks indicate the level of significance (*=significant to ****=highly significant).

FIG. 15 depicts mean HI titres (Log 2) (with standard deviation) results for ODN1 (GCGT3-TG4T-5Chol) during the entire study.

FIG. 16 depicts mean HI titres (Log 2) (with standard deviation) results for ODN2 (GCGT3-TG4T) at days 14 (top panel) and 21 (bottom panel) post vaccination. Asterisks indicate the level of significance (*=significant to ****=highly significant).

FIG. 17 depicts mean HI titres (Log 2) (with standard deviation) results for ODN2 (GCGT3-TG4T) during the entire study.

FIG. 18 depicts mean HI titres (Log 2) (with standard deviation) results for ODN3 (2006-PTO) at days 14 (top panel) and 21 (bottom panel) post vaccination. Asterisks indicate the level of significance (*=significant to ****=highly significant).

FIG. 19 depicts mean HI titres (Log 2) (with standard deviation) results for ODN3 (2006-PTO) during the entire study.

FIG. 20 depicts mean HI titres (Log 2) (with standard deviation) results for positive and negative control Test Articles at days 14 (top panel) and 21 (bottom panel) post vaccination. Asterisks indicate the level of significance (*=significant to ****=highly significant).

FIG. 21 depicts mean HI titres (Log 2) (with standard deviation) results for positive and negative control Test Articles during the entire study.

FIG. 22 depicts mean HI titres (Log 2) (with standard deviation) results at the most optimal concentrations of ODNs during the entire study compared to NDV vaccine alone.

FIG. 23 depicts mean HI titres (Log 2) (with standard deviation) results at the most optimal concentrations of ODNs at day 14 (top panel) and 21 (bottom panel) pv compared to NDV vaccine alone.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The disclosed compositions and methods may be understood more readily by reference to the following detailed description taken in connection with the accompanying figures, which form a part of this disclosure. It is to be understood that the disclosed compositions and methods are not limited to the specific compositions and methods described and/or shown herein, and that the terminology used herein is for the purpose of describing particular embodiments by way of example only and is not intended to be limiting of the claimed compositions and methods.

Unless specifically stated otherwise, any description as to a possible mechanism or mode of action or reason for improvement is meant to be illustrative only, and the disclosed compositions and methods are not to be constrained by the correctness or incorrectness of any such suggested mechanism or mode of action or reason for improvement.

Throughout this text, the descriptions refer to compositions and methods of using said compositions. Where the disclosure describes or claims a feature or embodiment associated with a composition, such a feature or embodiment is equally applicable to the methods of using said composition. Likewise, where the disclosure describes or claims a feature or embodiment associated with a method of using a composition, such a feature or embodiment is equally applicable to the composition.

When a range of values is expressed, another embodiment includes from the one particular value and/or to the other particular value. Further, reference to values stated in ranges include each and every value within that range. All ranges are inclusive and combinable. When values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another embodiment. Reference to a particular numerical value includes at least that particular value, unless the context clearly dictates otherwise.

It is to be appreciated that certain features of the disclosed compositions and methods which are, for clarity, described herein in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the disclosed compositions and methods that are, for brevity, described in the context of a single embodiment, may also be provided separately or in any subcombination.

As used herein, the singular forms “a,” “an,” and “the” include the plural.

“Co-administered” as used herein refers to administering the immunomodulatory composition in combination with the immunostimulatory oligonucleotide to achieve the desired immunostimulatory effect. The immunomodulatory composition and the immunostimulatory oligonucleotide can be co-administered as separate compositions or together as a single composition. If the immunomodulatory composition and the immunostimulatory oligonucleotide are separate compositions, they can be co-administered either simultaneously or sequentially in either order. For sequential co-administration, there may be a delay of a minute, an hour, or even one or more days between the administration of the immunomodulatory composition and the immunostimulatory oligonucleotide.

As used herein, “fusing” refers to creating a chemical bond between two chemically reactive species. In the context of this disclosure, fusing most often refers to incorporating specific elements into an oligonucleotide. For example, a run of thymine nucleotides can be fused to the 3′ end of an oligonucleotide.

As used herein, “G-quartet sequence” refers to a stretch of consecutive guanine residues near the 5′ end of an oligonucleotide that enables the oligonucleotide to interact with other G-quartet sequences to form a G-quartet. The G-quartet enhances the immunostimulatory properties of the nucleic acid. For example, oligonucleotides comprising G-quartet sequences may interact, resulting in G-quartets. G-quartet sequences occurring in the promoter region of a gene may form quaternary structures involved in regulating the expression of the gene. While a G-quartet sequence is not limited to any particular sequence, an example of a G-quartet sequence is TGGGGT.

As used herein, “G-wire sequence,” “G wire sequence,” “Gwire sequence,” and related terms, refer to a plurality, most often two, of at least four consecutive guanine nucleotides. The pluralities of guanine nucleotides, located at or near the 5′ terminus of an oligonucleotide, are separated by two or more non-guanine nucleotides (i.e., thymine). G-wire sequences are capable of interacting with other G-wire sequences to form a G-wire structure. A G-wire structure can enhance the immunostimulatory properties of a nucleic acid. An exemplary G-wire sequence is GGGGTTGGGG (SEQ ID NO: 257) or GGGGTTGGGGTTTT (SEQ ID NO: 258).

As used herein, the terms “guanine nucleotide enriched sequence,” “guanine enriched sequence,” and the like, refer to sequences comprising either a run of consecutive guanine nucleotides, usually between four to six guanine nucleotides, or a region of a nucleic acid, typically at or near the 5′ end of an oligonucleotide having more guanine nucleotides than adenine, cytosine, or thymine nucleotides. A guanine enriched sequence as disclosed herein can enhance the immunostimulatory properties of an oligonucleotide. G-quartet and G-wire sequences are both types of guanine nucleotide enriched sequences.

The term “immunomodulatory composition” as used herein refers to a composition comprising at least an immunogenic nucleic acid plasmid and a liposomal delivery vehicle. In some aspects of the presently disclosed compositions and methods, the nucleic acid plasmid may not code for a particular immunogen and may be immunogenic based on the inherent properties of the nucleic acid plasmid. In some aspects, the liposomal delivery vehicle is cationic.

An “immunogenic nucleic acid plasmid” is a nucleic acid plasmid that, when detected by a vertebrate immune system, elicits an immune response. Some immunogenic nucleic acid plasmids comprise an increased percentage of CpG dinucleotide motifs compared to nucleic acid plasmid sequences naturally occurring in some vertebrate organisms. Without being bound to theory, it is believed that increased CpG dinucleotide motifs are present in bacterially derived nucleic acid, and therefore, such CpG-enriched nucleic acid appears foreign to host immune defenses. Immunogenic nucleic acid plasmids can comprise non-naturally occurring nucleotides and derivatives of nucleotides.

“Immunostimulatory composition” as used herein refers to a composition comprising an immunomodulatory composition and an immunostimulatory oligonucleotide. In some aspects, the immunostimulatory oligonucleotide and the immunomodulatory composition comprise a single formulation that is the immunostimulatory composition. In some aspects, the immunostimulatory oligonucleotide may be physically associated with the liposomal delivery vehicle of the immunomodulatory composition.

As used herein, “inserting” refers to adding specific nucleotide(s) at specific positions during the synthesis of an oligonucleotide.

As used herein, “parallel orientation” refers to the directional interaction between different oligonucleotides. For example, individual oligonucleotides oriented in the same 5′ to 3′ direction are in a parallel orientation.

As used herein, “percent identity” and like terms are used to describe the sequence relationships between two or more nucleic acids, polynucleotides, proteins, or polypeptides, and are understood in the context of and in conjunction with the terms including: (a) reference sequence, (b) comparison window, (c) sequence identity and (d) percentage of sequence identity.

-   -   (a) A “reference sequence” is a defined sequence used as a basis         for sequence comparison. A reference sequence may be a subset of         or the entirety of a specified sequence; for example, a segment         of a full-length cDNA or gene sequence, or the complete cDNA or         gene sequence.     -   (b) A “comparison window” includes reference to a contiguous and         specified segment of a polynucleotide sequence, wherein the         polynucleotide sequence may be compared to a reference sequence         and wherein the portion of the polynucleotide sequence in the         comparison window may comprise additions, substitutions, or         deletions (i.e., gaps) compared to the reference sequence (which         does not comprise additions, substitutions, or deletions) for         optimal alignment of the two sequences. Those of skill in the         art understand that to avoid a misleadingly high similarity to a         reference sequence due to inclusion of gaps in the         polynucleotide sequence a gap penalty is typically introduced         and is subtracted from the number of matches.     -   (c) Methods of alignment of sequences for comparison are well         known in the art. Optimal alignment of sequences for comparison         may be conducted by the local homology algorithm of Smith and         Waterman, Adv. Appl. Math., 2: 482, 1981; by the homology         alignment algorithm of Needleman and Wunsch, J. Mol. Biol., 48:         443, 1970; by the search for similarity method of Pearson and         Lipman, Proc. Natl. Acad. Sci. USA, 8: 2444, 1988; by         computerized implementations of these algorithms, including, but         not limited to: CLUSTAL in the PC/Gene program by         Intelligenetics, Mountain View, Calif., GAP, BESTFIT, BLAST,         FASTA, and TFASTA in the Wisconsin Genetics Software Package,         Genetics Computer Group (GCG), 7 Science Dr., Madison, Wis.,         USA; the CLUSTAL program is well described by Higgins and Sharp,         Gene, 73: 237-244, 1988; Corpet, et al., Nucleic Acids Research,         16:881-90, 1988; Huang, et al., Computer Applications in the         Biosciences, 8:1-6, 1992; and Pearson, et al., Methods in         Molecular Biology, 24:7-331, 1994. The BLAST family of programs         which may be used for database similarity searches includes:         BLASTN for nucleotide query sequences against nucleotide         database sequences; BLASTX for nucleotide query sequences         against protein database sequences; TBLASTN for protein query         sequences against nucleotide database sequences; and TBLASTX for         nucleotide query sequences against nucleotide database         sequences. See, Current Protocols in Molecular Biology, Chapter         19, Ausubel, et al., Eds., Greene Publishing and         Wiley-Interscience, New York, 1995. New versions of the above         programs or new programs altogether will undoubtedly become         available in the future, and may be used with the present         disclosure.     -   (d) “Percent identity” means the value determined by comparing         two optimally aligned sequences over a comparison window,         wherein the portion of the polynucleotide sequence in the         comparison window may comprise additions, substitutions, or         deletions (i.e., gaps) as compared to the reference sequence         (which does not comprise additions, substitutions, or deletions)         for optimal alignment of the two sequences. The percentage is         calculated by determining the number of positions at which the         identical nucleic acid base occurs in both sequences to yield         the number of matched positions, dividing the number of matched         positions by the total number of positions in the window of         comparison and multiplying the result by 100 to yield the         percentage of sequence identity.

“Therapeutically effective amount” refers to an amount of an immunomodulatory composition and/or an immunostimulatory oligonucleotide or of an immunostimulatory composition that treats the subject.

“Synergistically effective amount” refers to an amount of an immunomodulatory composition and an immunostimulatory oligonucleotide that provides a synergistic, or more than additive, effect in treating the subject. The term “subject” as used herein is intended to mean any animal, but in particular, avian species. “Avian species” includes, but is not limited to, chickens, domestic turkeys, waterfowl and any other food source fowl.

As used herein, “treating” and like terms refer to reducing the severity and/or frequency of symptoms of an infection, eliminating symptoms and/or the underlying cause of said symptoms, reducing the frequency or likelihood of symptoms and/or their underlying cause, and/or improving or remediating damage caused, directly or indirectly, by an infectious agent.

Various terms relating to aspects of the description are used throughout the specification and claims. Such terms are to be given their ordinary meaning in the art unless otherwise indicated. Other specifically defined terms are to be construed in a manner consistent with the definitions provided herein.

Immunostimulatory compositions are provided herein comprising an immunomodulator composition comprising a nucleic acid plasmid and a liposomal delivery vehicle and an immunostimulatory oligonucleotide having at least one CpG motif and an guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide.

Immunostimulatory oligonucleotides, as described herein, can interact with TLR21 to elicit an immune response. The immunostimulatory oligonucleotides comprise at least one unmethylated dinucleotide CpG motif, which interacts with pathogen recognition receptors expressed in the host organism. The immunostimulatory oligonucleotides also have a guanine nucleotide enriched sequence. These sequences can facilitate the folding of a DNA strand into a quaternary structure or promote the aggregation of one or more immunostimulatory oligonucleotides that have an enhanced guanine the sequence. The guanine enriched sequence need not be comprised solely of guanine nucleotides, but it must be enriched. A guanine enriched sequence, as described supra and exemplified throughout these disclosures, typically is located at or near (within four nucleotides of) the oligonucleotide terminus. Additional manipulation of the oligonucleotide sequence and structure can further enhance the immunostimulatory oligonucleotide's ability to stimulate TLR21. Therefore, one embodiment of the present disclosure comprises an immunostimulatory composition comprising at least one immunostimulatory oligonucleotide having at least one CpG motif and a guanine enriched sequence beginning at or within four nucleotides of the 5′ terminus of the immunostimulatory oligonucleotide.

In some aspects of the present disclosure, the addition of guanine nucleotide runs to the 5′ end of the CpG containing immunostimulatory oligonucleotide can significantly improve immunogenicity of the immunostimulatory oligonucleotide. Not only does the position of the guanine rich sequence in the immunostimulatory oligonucleotide affect enhancement of TLR21 activation, but the content of the sequence has an effect as well. For this reason, in some aspects of the present disclosure, guanine enriched sequences comprise a plurality of consecutive guanine nucleotides.

In some embodiments, the guanine enriched sequence comprises a first plurality of consecutive guanine nucleotides. In some aspects the first plurality of guanine nucleotides comprises two to eight guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises two guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises three guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises four guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises five guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises six guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises seven guanine nucleotides. In some aspects, the first plurality of guanine nucleotides comprises eight guanine nucleotides. In still other aspects, the first plurality of guanine nucleotides comprises more than eight guanine nucleotides.

In some embodiments of the present invention, the oligonucleotide comprises SEQ ID NO:16, 17, 18, 19, 20, 21, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 77, 78, 81, 82, 85, 86, 89, 90, 92, 93, 96, 97, 100, 102, 104, 106, 108, or 143. In other embodiments, the guanine enriched sequence comprises TTAGGG, TTAGGGTTAGGG (SEQ ID NO:261), TTTTGGGG, GGGGTTTT, GGGGTTTTGGGG (SEQ ID NO:262), TTAGGG, TTAGGGTTAGGGTTTT (SEQ ID NO:263), TGTGGGTGTGTGTGGG (SEQ ID NO:269), GGAGG, TGGAGGC, or TGGAGGCTGGAGGC (SEQ ID NO:264). In still other embodiments, the oligonucleotide comprises SEQ ID NO:110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 124, 125, 126, 127, 129, 130, 131, 134, 136, 137, or 138.

A single run of guanine nucleotides is not the only 5′ modification that can enhance TLR21 stimulation. For example, adenine, cytosine, and thymine enriched sequences can also be added to the 5′ end of an oligonucleotide having CpG motif and result in enhanced TLR21 stimulation, albeit less than that elicited by the guanine enriched sequences at the 5′ end of the oligonucleotide. While a single plurality of guanine residues at the 5′ end of the oligonucleotide can elicit TLR21 stimulation, additional pluralities of guanine nucleotides in the guanine enriched sequence may further enhance the stimulatory properties of the oligonucleotide. Thus, in some aspects, the oligonucleotide of the present disclosure comprises a second plurality of guanine nucleotides between the first plurality of guanine nucleotides and the at least one CpG motif.

In some aspects, a plurality of guanine nucleotides comprises a G-quartet sequence. In some embodiments, the first plurality of guanine nucleotides, the second plurality of guanine nucleotides, or both comprise a G-quartet sequence. G-quartet sequences, as defined above, also allow for interaction between oligonucleotides. Without being bound by theory, interaction at the 5′ end of the oligonucleotides allows for the concentration of CpG dinucleotide motifs and a corresponding enhanced opportunity for recognition by TRL21. In some embodiments, the immunostimulatory composition further comprises at least one additional oligonucleotide having a G-quartet sequence, wherein the oligonucleotide and the at least one additional oligonucleotide have a parallel orientation in a quaternary structure. In some aspects, the G-quartet sequence comprises TGGGGT.

Another guanine enriched sequence that can be added at or near the 5′ terminus of an oligonucleotide having CpG motifs is a G-wire sequence. In some aspects of the present disclosure, the first and second pluralities of guanine nucleotides comprise a G-wire sequence. In some aspects, the G-wire sequence comprises SEQ ID NO:257 or 258. In still other aspects, the G-wire sequence comprises SEQ ID NO:141, 142, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, or GCGT-Gwire3. The two pluralities of guanine nucleotides can be separated by non-guanine nucleotides, nucleotide analogs, or any other spacer or linker. For example, in some aspects of the present disclosure, the first plurality of guanine nucleotides and the second plurality of guanine nucleotides are separated by at least one nucleotide. As used herein, the term “spacer” refers to a chemical linkage between similar nucleotide motifs, i.e., between two CpG motifs or between two guanine nucleotide enriched sequence motifs, whereas the term “linker” refers to a chemical linkage between different nucleotide motifs, i.e., between a guanine nucleotide enriched sequence and another nucleotide motif, e.g., a CpG motif. The terms “spacer” and “linker” are used for clarity in describing which aspect of an oligonucleotide is being discussed. However, it will be understood by those skilled in the art that the structures disclosed herein for spacers can be interchangeable with the structures disclosed herein for linkers, and vice versa.

Without being bound by any particular theory, it is possible that the G-wire sequence enables an oligonucleotide to interact and aggregate with other oligonucleotides having G-wire sequences. The conformation assumed by the aggregation of oligonucleotides having G-wire sequences is referred to as G-wire conformation, and this accumulation of oligonucleotides and their CpG motifs can lead to enhanced stimulation of TLR21.

The guanine enriched sequences may be separated from the CpG nucleotide motifs by nucleotides, nucleotide analogs, or other linkers. Therefore, in some embodiments of the present disclosure, the oligonucleotide further comprises a linker between the guanine enriched sequence and the downstream at least one CpG motif. As used herein, “downstream” means in the 5′→3′ direction; i.e., a “downstream” nucleotide or motif is a nucleotide or motif that is 3′ of a comparison sequence element. “Upstream” means in the 3′→5′ direction; i.e., an “upstream” nucleotide or motif is a nucleotide or motif that is 5′ of a comparison sequence element. The linker need not be directly adjacent to either the guanine enriched sequence or the CpG motif; rather, the linker must reside between the two sequence motifs regardless of intervening sequences between the guanine enriched sequence and the linker, as well as between the CpG motif and the linker. In some embodiments of the present disclosures, the linker comprises at least three nucleotides. The linker also may not comprise nitrogenous bases. For example, in some aspects, the linker is a hexaethyleneglycol, a propanediol, a triethyleneglycol, or derivatives thereof. In other examples, the oligonucleotide having a linker comprises 2006-PDE5dG4-X1 or 2006-PDE5dG4-X3.

Dinucleotide CpG motifs present in the oligonucleotides of the present disclosure are believed to be PAMPs recognized by TLR21 in chickens. While even a single CpG motif can stimulate TLR21, multiple CpGs present on an oligonucleotide can increase stimulated TLR21 signal strength. For this reason, in some aspects of the present invention, the at least one CpG motif comprises two, three, four, or five CpG motifs. In some aspects the at least one CpG motif comprises six or more CpG motifs. In some aspects, the at least one CpG motif comprises two CpG motifs. In some aspects, the at least one CpG motif comprises three CpG motifs. In some aspects, the at least one CpG motif comprises four CpG motifs. In some embodiments, the at least one CpG motif comprises four CpG motifs.

In some embodiments of the presently disclosed oligonucleotides, each CpG motif may be separated from the other CpG motifs by at least one nucleotide or nucleotide analog. In some aspects, the at least one nucleotide is two or three thymine nucleotides. In other aspects, the at least one nucleotide is between one and four nucleotides, although the number of intervening nucleotides may differ depending on the sequence of the intervening nucleotides. In some aspects, the oligonucleotide comprises SEQ ID NO:217, 218, 219, or 220. The nucleotides adjacent to a CpG—along with the CpG motif itself—constitute a CpG sequence element (e.g., XCGX, where X=any nucleotide). The oligonucleotides of the present disclosure, in some aspects comprise CpG sequence elements that are GCGA, GCGG, ACGC, CCGC, GCGT, TCGC, or any combination thereof.

In some embodiments of the present disclosures, the CpG motif comprises a CpG sequence element having four nucleotides. In some aspects, the oligonucleotide comprises at least two CpG sequence elements. In some aspects, the oligonucleotide comprises at least three CpG sequence elements. In some aspects, the oligonucleotide comprises at least four CpG sequence elements. In some aspects, the oligonucleotide comprises at least five CpG sequence elements. In some aspects, the oligonucleotide comprises at least six CpG sequence elements. In some aspects, the oligonucleotide comprises more than eight, ten, fifteen, or even twenty CpG sequence elements.

In other embodiments of the presently disclosed oligonucleotides, each of the CpG motifs are separated from every other CpG motif by a spacer or a combination of a spacer and at least one nucleotide. In some aspects, at least one CpG motif is separated from the nearest other CpG motif by a spacer or a combination of a spacer and at least one nucleotide, while at least two other CpG motifs are adjacent to each other. Although separated CpG motifs may enhance the immunostimulatory capabilities of the designed oligonucleotides, it is acknowledged that CpG motifs adjacent to each other can still stimulate TLR21.

The spacer employed to linearly separate CpG motifs can be any linkage that bridges at least a portion of the oligonucleotide between the CpG motifs. The spacer may be comprised of, but not necessarily limited to, a deoxyribose phosphate bridge, a multiple carbon chain, or a repeated chemical unit. One essential property of a spacer is the ability to form a chemical bond with the nucleotide backbone of the oligonucleotide. Therefore, in some embodiments the spacer is a deoxyribose phosphate bridge. The deoxyribose phosphate bridge may comprise nitrogenous bases in some aspects while in others the deoxyribose phosphate bridge is abasic. In some aspects, the oligonucleotide comprises SEQ ID NO:221, which comprises an abasic deoxyribose phosphate bridge.

In other embodiments of the present disclosure, the spacer comprises a carbon chain. The carbon chain can comprise two to twelve carbon atoms. Diols comprising a carbon chain can be used as the terminal alcohol groups can react with terminal alcohol and/or phosphate groups of an oligonucleotide. In some embodiments, the carbon chain comprises two carbon atoms, and in some aspects, the carbon chain is derived from ethanediol. In some embodiments, the oligonucleotide comprises ODN-X2, wherein X2 is ethanediol.

Other embodiments of the present disclosure provide for the carbon chain comprising three carbon atoms. In some aspects of these embodiments, the carbon chain is derived from 1,3-propanediol. In some embodiments, the oligonucleotide comprises CG-Gw2X2, CG-Gw2X2-2, or ODN-X3, CG-Gw2X2-1, CG-Gw2X2-3, CG-Gw2X2-4, CG-Gw2X2-5, CG-G4T16X2-1, CG-G4T16X2-2, CG-G4T16X2-3, CG-G4T16X2-4, or CG-G4T16X2-5, wherein X2 is a three carbon chain; 2006-PDE5dG4-X2 wherein X2 is a three carbon chain derived from propanediol; or SEQ ID NO:250, wherein X4 is a three carbon chain derived from propanediol.

In yet other embodiments of the present disclosure the oligonucleotide comprises a carbon chain spacer, wherein the carbon chain comprises four carbon atoms. In some aspects of these embodiments, the carbon chain is derived from 1,4-butanediol. In some embodiments, the oligonucleotide comprises ODN-X4, wherein X4 is a four carbon chain derived from 1,4-butanediol.

In still other embodiments of the present disclosures, the oligonucleotide comprises a spacer having a repeated chemical unit. For example, in some embodiments, the repeated chemical unit is an ethylene glycol. The repeated chemical unit may be repeated two to twelve times. In some embodiments, ethylene glycol is repeated six times. Thus, in some aspects, the oligonucleotide comprises CCGC-Gw2X1, wherein X1 is a spacer derived from hexaethyleneglycol.

Although guanine nucleotide runs on the 3′ terminus of an oligonucleotide results in little, if any, TLR21 stimulation, other nucleotide runs can impart enhanced immunogenicity to the oligonucleotide. Specifically, in some aspects of the present disclosures, the oligonucleotide may further comprise a tri-thymine nucleotide 3′ terminal end. In some aspects, the oligonucleotide comprises SEQ ID NO:204, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, or 215.

For each oligonucleotide disclosed herein, one skilled in the art would know that a nucleotide can be substituted with a nucleotide analog. The oligonucleotides in some embodiments comprise a phosphodiester backbone, although other embodiments of the oligonucleotides disclosed herein comprise a phosphorothioate backbone. Phosphorothioate backbones may, in some circumstances, be easier and more cost effective to manufacture.

In some embodiments of the present disclosure, the oligonucleotide may comprise a lipid moiety, which can lead to an increase in the oligonucleotide's immunogenicity. One possible explanation for the increased immunogenicity is that the lipid moiety may function to enhance the bioavailability of the oligonucleotide. In some embodiments, the lipid moiety is at or near the 5′ terminus of the oligonucleotide. This lipid “cap” may prevent degradation, increase solubility, improve the oligonucleotide's stability in a pharmaceutical composition, or any combination thereof. In some aspects, the lipid moiety is a cholesteryl.

The potency of the immunostimulatory oligonucleotide and the immunostimulatory composition can be characterized by their half-maximum effective concentration (EC₅₀), which is a measurement of the concentration necessary to induce a response that is half of the maximum response that can be attained by administering the composition. The lower the concentration, the more potent the oligonucleotide. In some aspects of the present disclosures, the immunostimulatory composition can have an EC₅₀ in the pM range. In some aspects, the EC₅₀ is between about 0.1 and 100 pM. In some aspects, the EC₅₀ is between about 100 and 200 pM. In some aspects the EC₅₀ is between about 200 and 300 pM. In some aspects, the EC₅₀ is between about 300 and 400 pM. In some aspects the EC₅₀ is between about 400 and 500 pM. In some aspects the EC₅₀ is between about 500 and 600 pM. In some aspects the EC₅₀ is between about 600 and 700 pM. In some aspects the EC₅₀ is between about 700 and 800 pM. In some aspects the EC₅₀ is between about 800 and 900 pM. In some aspects the EC₅₀ is between about 900 and 1 nM. In still other aspects, the EC₅₀ is less than about 100 pM.

Regarding the concentration of the oligonucleotide in the immunostimulatory composition, in some aspects the concentration of the oligonucleotide is between about 0.1 and 10 nM. In some aspects, the concentration of the oligonucleotide is between about 10 and 20 nM. In some aspects the concentration of the oligonucleotide is between about 20 and 30 nM. In some aspects, the concentration of the oligonucleotide is between about 30 and 40 nM. In some aspects the concentration of the oligonucleotide is between about 40 and 50 nM. In some aspects the concentration of the oligonucleotide is between about 50 and 60 nM. In some aspects the concentration of the oligonucleotide is between about 60 and 70 nM. In some aspects the concentration of the oligonucleotide is between about 70 and 80 nM. In some aspects the concentration of the oligonucleotide is between about 80 and 90 nM. In some aspects the concentration of the oligonucleotide is between about 90 and 100 nM. In still other aspects, the concentration of the oligonucleotide is less than about 20 nM.

The immunostimulatory composition may further comprise at least one additional oligonucleotide having a G-wire sequence in some embodiments of the present disclosure. Because the G-wire sequence facilitates the aggregation of other oligonucleotides having the same, or similar, G-wire sequence, one aspect of the immunostimulatory composition further comprises at least one additional oligonucleotide having a G-wire sequence. In some aspects in which the immunostimulatory composition comprises multiple oligonucleotides having G-wire sequences, the oligonucleotide and the at least one additional oligonucleotide have a G-wire conformation.

The ability of an oligonucleotide to stimulate TLR21 may be further enhanced according to some aspect of the invention by inserting additional CpG motifs. In some aspects, the at least one CpG motif is a plurality of CpG motifs, and the plurality of CpG motifs comprises two, three, four, or five CpG motifs. Distance between the CpG motifs can influence the oligonucleotide's TLR21 stimulatory properties. For this reason, some aspects of the disclosed oligonucleotides provide for insertion of at least one nucleotide or nucleotide analog between the CpG motifs. The at least one nucleotide may be two or three thymine nucleotides.

Other embodiments provide for inclusion of a spacer between each of the CpG motifs. The spacer must be able to bond to the 3′ terminus of one adjacent nucleotide strand and to the 5′ end of the other nucleotide strand. In some aspects, the spacer is a deoxyribose phosphate bridge, which can be abasic in some aspects.

The spacer, in some aspects, may comprise a carbon chain. In some embodiments the carbon chain comprises two carbon atoms. In some aspects the carbon chain is derived from ethanediol. Other embodiments provide for a carbon chain comprising three carbon atoms. In some aspects, the carbon chain is derived from 1,3-propanediol. In some embodiments, the carbon chain comprises four carbon atoms, and in some aspects the carbon chain is derived from 1,4-butanediol. In still other embodiments, the spacer comprises a repeated chemical unit. In some aspects, the repeated chemical unit is an ethylene glycol, and in some aspects the spacer is derived from hexaethyleneglycol.

Representative oligonucleotides of the present disclosure are identified in Table 1.

TABLE 1 Oligonucleotide sequences 5Chol-GCGT3- SEQ ID NO: 1 XTGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT TG4T X = 5′-Cholesteryl 2006-PTO SEQ ID NO: 3 tcgtcgttttgtcgttttgtcgtt 2006-PDE SEQ ID NO: 4 TCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE3dG1 SEQ ID NO: 5 TCGTCGTTTTGTCGTTTTGTCGTTG 2006-PDE3dG2 SEQ ID NO: 6 TCGTCGTTTTGTCGTTTTGTCGTTGG 2006-PDE3dG3 SEQ ID NO: 7 TCGTCGTTTTGTCGTTTTGTCGTTGGG 2006-PDE3dG4 SEQ ID NO: 8 TCGTCGTTTTGTCGTTTTGTCGTTGGGG 2006-PDE3dG5 SEQ ID NO: 9 TCGTCGTTTTGTCGTTTTGTCGTTGGGGG 2006-PDE3dG6 SEQ ID NO: 10 TCGTCGTTTTGTCGTTTTGTCGTTGGGGGG 2006-PDE3dG7 SEQ ID NO: 11 TCGTCGTTTTGTCGTTTTGTCGTTGGGGGGG 2006-PDE3dG8 SEQ ID NO: 12 TCGTCGTTTTGTCGTTTTGTCGTTGGGGGGGG 2006-PTO SEQ ID NO: 3 tcgtcgttttgtcgttttgtcgtt 2006-PDEV3 SEQ ID NO: 13 TCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG1 SEQ ID NO: 14 GTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG2 SEQ ID NO: 15 GGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG3 SEQ ID NO: 16 GGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG4 SEQ ID NO: 17 GGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG5 SEQ ID NO: 18 GGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG6 SEQ ID NO: 19 GGGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG7 SEQ ID NO: 20 GGGGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG8 SEQ ID NO: 21 GGGGGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dA6 SEQ ID NO: 22 AAAAAATCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dC6 SEQ ID NO: 23 CCCCCCTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dT6 SEQ ID NO: 24 TTTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE5dG6- SEQ ID NO: 25 GGGGGGTm5cGTm5cGTTTTGTm5cGTTTTGTm5cGTT Me m5c = 5-methyl-cytidine 2006-PDE5dC6- SEQ ID NO: 26 CCCCCCTGCTGCTTTTGTGCTTTTGTGCTT GC 2006-PDE5dT6- SEQ ID NO: 27 TTTTTTTCATCATTTTGTCATTTTGTCATT CA 2006-PTO3dG5 SEQ ID NO: 28 tgggggtcgtcgttttgtcgttttgtcgtt 2006-PTO5dG6 SEQ ID NO: 29 tcgtcgttttgtcgttttgtcgttggggg 2006-PDE5dG6- SEQ ID NO: 30 AGGGGGTCGTCGTTTTGTCGTTTTGTCGTT A1 2006-PDE5dG6- SEQ ID NO: 31 GAGGGGTCGTCGTTTTGTCGTTTTGTCGTT A2 2006-PDE5dG6- SEQ ID NO: 32 GGAGGGTCGTCGTTTTGTCGTTTTGTCGTT A3 2006-PDE5dG6- SEQ ID NO: 33 GGGAGGTCGTCGTTTTGTCGTTTTGTCGTT A4 2006-PDE5dG6- SEQ ID NO: 34 GGGGAGTCGTCGTTTTGTCGTTTTGTCGTT A5 2006-PDE5dG6- SEQ ID NO: 35 GGGGGATCGTCGTTTTGTCGTTTTGTCGTT A6 2006-PDE5dG6- SEQ ID NO: 36 AAGGGGTCGTCGTTTTGTCGTTTTGTCGTT A12 2006-PDE5dG6- SEQ ID NO: 37 GAAGGGTCGTCGTTTTGTCGTTTTGTCGTT A23 2006-PDE5dG6- SEQ ID NO: 38 GGAAGGTCGTCGTTTTGTCGTTTTGTCGTT A34 2006-PDE5dG6- SEQ ID NO: 39 GGGAAGTCGTCGTTTTGTCGTTTTGTCGTT A45 2006-PDE5dG6- SEQ ID NO: 40 GGGGAATCGTCGTTTTGTCGTTTTGTCGTT A56 2006-PDE5dG6- SEQ ID NO: 41 CGGGGGTCGTCGTTTTGTCGTTTTGTCGTT C1 2006-PDE5dG6- SEQ ID NO: 42 GCGGGGTCGTCGTTTTGTCGTTTTGTCGTT C2 2006-PDE5dG6- SEQ ID NO: 43 GGCGGGTCGTCGTTTTGTCGTTTTGTCGTT C3 2006-PDE5dG6- SEQ ID NO: 44 GGGCGGTCGTCGTTTTGTCGTTTTGTCGTT C4 2006-PDE5dG6- SEQ ID NO: 45 GGGGCGTCGTCGTTTTGTCGTTTTGTCGTT C5 2006-PDE5dG6- SEQ ID NO: 46 GGGGGCTCGTCGTTTTGTCGTTTTGTCGTT C6 2006-PDE5dG6- SEQ ID NO: 47 CCGGGGTCGTCGTTTTGTCGTTTTGTCGTT C12 2006-PDE5dG6- SEQ ID NO: 48 GCCGGGTCGTCGTTTTGTCGTTTTGTCGTT C23 2006-PDE5dG6- SEQ ID NO: 49 GGCCGGTCGTCGTTTTGTCGTTTTGTCGTT C34 2006-PDE5dG6- SEQ ID NO: 50 GGGCCGTCGTCGTTTTGTCGTTTTGTCGTT C45 2006-PDE5dG6- SEQ ID NO: 51 GGGGCCTCGTCGTTTTGTCGTTTTGTCGTT C56 2006-PDE5dG6- SEQ ID NO: 52 TGGGGGTCGTCGTTTTGTCGTTTTGTCGTT T1 2006-PDE5dG6- SEQ ID NO: 53 GTGGGGTCGTCGTTTTGTCGTTTTGTCGTT T2 2006-PDE5dG6- SEQ ID NO: 54 GGTGGGTCGTCGTTTTGTCGTTTTGTCGTT T3 2006-PDE5dG6- SEQ ID NO: 55 GGGTGGTCGTCGTTTTGTCGTTTTGTCGTT T4 2006-PDE5dG6- SEQ ID NO: 56 GGGGTGTCGTCGTTTTGTCGTTTTGTCGTT T5 2006-PDE5dG6- SEQ ID NO: 57 GGGGGTTCGTCGTTTTGTCGTTTTGTCGTT T6 2006-PDE5dG6- SEQ ID NO: 58 TTGGGGTCGTCGTTTTGTCGTTTTGTCGTT T12 2006-PDE5dG6- SEQ ID NO: 59 GTTGGGTCGTCGTTTTGTCGTTTTGTCGTT T23 2006-PDE5dG6- SEQ ID NO: 60 GGTTGGTCGTCGTTTTGTCGTTTTGTCGTT T34 2006-PDE5dG6- SEQ ID NO: 61 GGGTTGTCGTCGTTTTGTCGTTTTGTCGTT T45 2006-PDE5dG6- SEQ ID NO: 62 GGGGTTTCGTCGTTTTGTCGTTTTGTCGTT T56 2006-PDE5dG4- SEQ ID NO: 63 AGGGTCGTCGTTTTGTCGTTTTGTCGTT A1 2006-PDE5dG4- SEQ ID NO: 64 GAGGTCGTCGTTTTGTCGTTTTGTCGTT A2 2006-PDE5dG4- SEQ ID NO: 65 GGAGTCGTCGTTTTGTCGTTTTGTCGTT A3 2006-PDE5dG4- SEQ ID NO: 66 GGGATCGTCGTTTTGTCGTTTTGTCGTT A4 2006-PDE5dG4- SEQ ID NO: 67 CGGGTCGTCGTTTTGTCGTTTTGTCGTT C1 2006-PDE5dG4- SEQ ID NO: 68 GCGGTCGTCGTTTTGTCGTTTTGTCGTT C2 2006-PDE5dG4- SEQ ID NO: 69 GGCGTCGTCGTTTTGTCGTTTTGTCGTT C3 2006-PDE5dG4- SEQ ID NO: 70 GGGCTCGTCGTTTTGTCGTTTTGTCGTT C4 2006-PDE5dG4- SEQ ID NO: 71 TGGGTCGTCGTTTTGTCGTTTTGTCGTT T1 2006-PDE5dG4- SEQ ID NO: 72 GTGGTCGTCGTTTTGTCGTTTTGTCGTT T2 2006-PDE5dG4- SEQ ID NO: 73 GGTGTCGTCGTTTTGTCGTTTTGTCGTT T3 2006-PDE5dG4- SEQ ID NO: 74 GGGTTCGTCGTTTTGTCGTTTTGTCGTT T4 1668 SEQ ID NO: 75 TCCATGACGTTCCTGATGCT 1668-3dG5 SEQ ID NO: 76 TCCATGACGTTCCTGATGCTGGGGG 1668-5dG4 SEQ ID NO: 77 GGGGTCCATGACGTTCCTGATGCT 1668-5dG6 SEQ ID NO: 78 GGGGGGTCCATGACGTTCCTGATGCT 1826 SEQ ID NO: 79 TCCATGACGTTCCTGACGTT 1826-3dG5 SEQ ID NO: 80 TCCATGACGTTCCTGACGTTGGGGG 1826-5dG4 SEQ ID NO: 81 GGGGTCCATGACGTTCCTGACGTT 1826-5dG6 SEQ ID NO: 82 GGGGGGTCCATGACGTTCCTGACGTT BW006 SEQ ID NO: 83 TCGACGTTCGTCGTTCGTCGTTC BW006-3dG5 SEQ ID NO: 84 TCGACGTTCGTCGTTCGTCGTTCGGGGG BW006-5dG4 SEQ ID NO: 85 GGGGTCGACGTTCGTCGTTCGTCGTTC BW006-5dG6 SEQ ID NO: 86 GGGGGGTCGACGTTCGTCGTTCGTCGTTC D-SLO1 SEQ ID NO: 87 TCGCGACGTTCGCCCGACGTTCGGTA D-SLO1-3dG5 SEQ ID NO: 88 TCGCGACGTTCGCCCGACGTTCGGTAGGGGG D-SLO1-5dG4 SEQ ID NO: 89 GGGGTCGCGACGTTCGCCCGACGTTCGGTA D-SLO1-5dG6 SEQ ID NO: 90 GGGGGGTCGCGACGTTCGCCCGACGTTCGGTA 2395 SEQ ID NO: 91 TCGTCGTTTTCGGCGCGCGCCG 2395-5dG4 SEQ ID NO: 92 GGGGTCGTCGTTTTCGGCGCGCGCCG 2395-5dG6 SEQ ID NO: 93 GGGGGGTCGTCGTTTTCGGCGCGCGCCG M362 SEQ ID NO: 94 TCGTCGTCGTTCGAACGACGTTGAT M362-3dG5 SEQ ID NO: 95 TCGTCGTCGTTCGAACGACGTTGATGGGGG M362-5dG4 SEQ ID NO: 96 GGGGTCGTCGTCGTTCGAACGACGTTGAT M362-5dG6 SEQ ID NO: 97 GGGGGGTCGTCGTCGTTCGAACGACGTTGAT 2007-PDE SEQ ID NO: 98 TCGTCGTTGTCGTTTTGTCGTT 2007-PDE3dG5 SEQ ID NO: 99 TCGTCGTTGTCGTTTTGTCGTTGGGGG 2007-PDE5dG6 SEQ ID NO: 100 GGGGGGTCGTCGTTGTCGTTTTGTCGTT CPG-202 SEQ ID NO: 101 GATCTCGCTCGCTCGCTAT CPG-202-5dG6 SEQ ID NO: 102 GGGGGGGATCTCGCTCGCTCGCTAT CPG-685 SEQ ID NO: 103 TCGTCGACGTCGTTCGTTCTC CPG-685-5dG6 SEQ ID NO: 104 GGGGGGTCGTCGACGTCGTTCGTTCTC CPG-2000 SEQ ID NO: 105 TCCATGACGTTCCTGCAGTTCCTGACGTT CPG-2000-5dG6 SEQ ID NO: 106 GGGGGGTCCATGACGTTCCTGCAGTTCCTGACGTT CPG-2002 SEQ ID NO: 107 TCCACGACGTTTTCGACGTT CPG-2002-5dG6 SEQ ID NO: 108 GGGGGGTCCACGACGTTTTCGACGTT 2006-T4-PDE SEQ ID NO: 109 TTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-HuTel-1 SEQ ID NO: 110 TTAGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-HuTel-2 SEQ ID NO: 111 TTAGGGTTAGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE-Oxy1 SEQ ID NO: 112 TTTTGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE-Oxy2 SEQ ID NO: 113 GGGGTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE-Oxy3 SEQ ID NO: 114 GGGGTTTTGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4-HuTel-1 SEQ ID NO: 115 TTAGGGTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4-HuTel-2 SEQ ID NO: 116 TTAGGGTTAGGGTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4-ScerTel SEQ ID NO: 117 TGTGGGTGTGTGTGGGTTTTTCGTCGTTTTGTCGTTTTGT CGTT 2006-T4-cMyc SEQ ID NO: 118 GGAGGTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4-cMyc2 SEQ ID NO: 119 TGGAGGCTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4-cMyc3 SEQ ID NO: 120 TGGAGGCTGGAGGCTTTTTCGTCGTTTTGTCGTTTTGTCG TT EA2-2006 SEQ ID NO: 121 GCTGCGAGGCGGGTGGGTGGGATCGTCGTTTTGTCGTTTT GTCGTT EA2D-2006 SEQ ID NO: 122 GCTGCGGGCGGGTGGGTGGGATCGTCGTTTTGTCGTTTTG TCGTT EA2a-2006 SEQ ID NO: 123 CGAGGCGGGTGGGTGGGATCGTCGTTTTGTCGTTTTGTCG TT EA2aD-2006 SEQ ID NO: 124 CGGGCGGGTGGGTGGGATCGTCGTTTTGTCGTTTTGTCGT T HCV-2006 SEQ ID NO: 125 GGGCGTGGTGGGTGGGGTTCGTCGTTTTGTCGTTTTGTCG TT HIV-93del-2006 SEQ ID NO: 126 GGGGTGGGAGGAGGGTTCGTCGTTTTGTCGTTTTGTCGTT Hema-2006 SEQ ID NO: 127 GGGGTCGGGCGGGCCGGGTGTCGTCGTTTTGTCGTTTTGT CGTT Insu-2006 SEQ ID NO: 128 GGTGGTGGGGGGGGTTGGTAGGGTTCGTCGTTTTGTCGTT TTGTCGTT IonK-2006 SEQ ID NO: 129 GGGTTAGGGTTAGGGTAGGGTCGTCGTTTTGTCGTTTTGT CGTT Scle-2006 SEQ ID NO: 130 TGGGGGGGTGGGTGGGTTCGTCGTTTTGTCGTTTTGTCGT T STAT-2006 SEQ ID NO: 131 GGGCGGGCGGGCGGGCTCGTCGTTTTGTCGTTTTGTCGTT TBA-2006 SEQ ID NO: 132 GGTTGGTGTGGTTGGTCGTCGTTTTGTCGTTTTGTCGTT TNF-2006 SEQ ID NO: 133 GGTGGATGGCGCAGTCGGTCGTCGTTTTGTCGTTTTGTCG TT apVEGF-D-2006 SEQ ID NO: 134 TGGGGGTGGACGGGCCGGGTTCGTCGTTTTGTCGTTTTGT CGTT apVEGF-2006 SEQ ID NO: 135 TGTGGGGGTGGACGGGCCGGGTTCGTCGTTTTGTCGTTTT GTCGTT HTR-2006 SEQ ID NO: 136 GGGTTAGGGTTAGGGTTAGGGTCGTCGTTTTGTCGTTTTG TCGTT bcl-2-2006 SEQ ID NO: 137 GGGCGCGGGAGGAAGGGGGCGGGTCGTCGTTTTGTCGTTT TGTCGTT c-myc-2006 SEQ ID NO: 138 AGGGTGGGGAGGGTGGGGATCGTCGTTTTGTCGTTTTGTC GTT c-kit87-2006 SEQ ID NO: 139 AGGGAGGGCGCTGGGAGGAGGGTCGTCGTTTTGTCGTTTT GTCGTT vegf-2006 SEQ ID NO: 140 GGGGCGGGCCGGGGGCGGGGTCGTCGTTTTGTCGTTTTGT CGTT 2006-PDE-Gwire1 SEQ ID NO: 141 GGGGTTGGGGTCGTCGTTTTGTCGTTTTGTCGTT 2006-PDE-Gwire2 SEQ ID NO: 142 GGGGTTGGGGTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006PDE5dG4- SEQ ID NO: 143 TGGGGTTCGTCGTTTTGTCGTTTTGTCGTT T1-6  1-ACGA SEQ ID NO: 144 TTTTTTTACGATTT  2-GCGA SEQ ID NO: 145 TTTTTTTGCGATTT  3-CCGA SEQ ID NO: 146 TTTTTTTCCGATTT  4-TCGA SEQ ID NO: 147 TTTTTTTTCGATTT  5-ACGG SEQ ID NO: 148 TTTTTTTACGGTTT  6-GCGG SEQ ID NO: 149 TTTTTTTGCGGTTT  7-CCGG SEQ ID NO: 150 TTTTTTTCCGGTTT  8-TCGG SEQ ID NO: 151 TTTTTTTTCGGTTT  9-ACGC SEQ ID NO: 152 TTTTTTTACGCTTT 10-GCGC SEQ ID NO: 153 TTTTTTTGCGCTTT 11-CCGC SEQ ID NO: 154 TTTTTTTCCGCTTT 12-TCGC SEQ ID NO: 155 TTTTTTTTCGCTTT 13-ACGT SEQ ID NO: 156 TTTTTTTACGTTTT 14-GCGT SEQ ID NO: 157 TTTTTTTGCGTTTT 15-CCGT SEQ ID NO: 158 TTTTTTTCCGTTTT 16-TCGT SEQ ID NO: 159 TTTTTTTTCGTTTT 17-ACGA-5dG6 SEQ ID NO: 160 GGGGGGTTTTTTTACGATTT 18-GCGA-5dG6 SEQ ID NO: 161 GGGGGGTTTTTTTGCGATTT 19-CCGA-5dG6 SEQ ID NO: 162 GGGGGGTTTTTTTCCGATTT 20-TCGA-5dG6 SEQ ID NO: 163 GGGGGGTTTTTTTTCGATTT 21-ACGG-5dG6 SEQ ID NO: 164 GGGGGGTTTTTTTACGGTTT 22-GCGG-5dG6 SEQ ID NO: 165 GGGGGGTTTTTTTGCGGTTT 23-CCGG-5dG6 SEQ ID NO: 166 GGGGGGTTTTTTTCCGGTTT 24-TCGG-5dG6 SEQ ID NO: 167 GGGGGGTTTTTTTTCGGTTT 25-ACGC-5dG6 SEQ ID NO: 168 GGGGGGTTTTTTTACGCTTT 26-GCGC-5dG6 SEQ ID NO: 169 GGGGGGTTTTTTTGCGCTTT 27-CCGC-5dG6 SEQ ID NO: 170 GGGGGGTTTTTTTCCGCTTT 28-TCGC-5dG6 SEQ ID NO: 171 GGGGGGTTTTTTTTCGCTTT 29-ACGT-5dG6 SEQ ID NO: 172 GGGGGGTTTTTTTACGTTTT 30-GCGT-5dG6 SEQ ID NO: 173 GGGGGGTTTTTTTGCGTTTT 31-CCGT-5dG6 SEQ ID NO: 174 GGGGGGTTTTTTTCCGTTTT 32-TCGT-5dG6 SEQ ID NO: 175 GGGGGGTTTTTTTTCGTTTT 33-ACGA-Gwire2 SEQ ID NO: 176 GGGGTTGGGGTTTTTTTTTTTACGATTT 34-GCGA-Gwire2 SEQ ID NO: 177 GGGGTTGGGGTTTTTTTTTTTGCGATTT 35-CCGA-Gwire2 SEQ ID NO: 178 GGGGTTGGGGTTTTTTTTTTTCCGATTT 36-TCGA-Gwire2 SEQ ID NO: 179 GGGGTTGGGGTTTTTTTTTTTTCGATTT 37-ACGG-Gwire2 SEQ ID NO: 180 GGGGTTGGGGTTTTTTTTTTTACGGTTT 38-GCGG-Gwire2 SEQ ID NO: 181 GGGGTTGGGGTTTTTTTTTTTGCGGTTT 39-CCGG-Gwire2 SEQ ID NO: 182 GGGGTTGGGGTTTTTTTTTTTCCGGTTT 40-TCGG-Gwire2 SEQ ID NO: 183 GGGGTTGGGGTTTTTTTTTTTTCGGTTT 41-ACGC-Gwire2 SEQ ID NO: 184 GGGGTTGGGGTTTTTTTTTTTACGCTTT 42-GCGC-Gwire2 SEQ ID NO: 185 GGGGTTGGGGTTTTTTTTTTTGCGCTTT 43-CCGC-Gwire2 SEQ ID NO: 186 GGGGTTGGGGTTTTTTTTTTTCCGCTTT 44-TCGC-Gwire2 SEQ ID NO: 187 GGGGTTGGGGTTTTTTTTTTTTCGCTTT 45-ACGT-Gwire2 SEQ ID NO: 188 GGGGTTGGGGTTTTTTTTTTTACGTTTT 46-GCGT-Gwire2 SEQ ID NO: 189 GGGGTTGGGGTTTTTTTTTTTGCGTTTT 47-CCGT-Gwire2 SEQ ID NO: 190 GGGGTTGGGGTTTTTTTTTTTCCGTTTT 48-TCGT-Gwire2 SEQ ID NO: 191 GGGGTTGGGGTTTTTTTTTTTTCGTTTT GCGT-Gwire2-GC SEQ ID NO: 192 GGGGTTGGGGTTTTTTTTTTTGGCTTTT GCGT-Gwire2-TG SEQ ID NO: 193 GGGGTTGGGGTTTTTTTTTTTGTGTTTT GCGT-Gwire2-CA SEQ ID NO: 194 GGGGTTGGGGTTTTTTTTTTTGCATTTT GCGT-Gwire2-T1 SEQ ID NO: 195 GGGGTTGGGGTTTTTTTTTTGCGTTTT GCGT-Gwire2-T2 SEQ ID NO: 196 GGGGTTGGGGTTTTTTTTTGCGTTTT GCGT-Gwire2-T3 SEQ ID NO: 197 GGGGTTGGGGTTTTTTTTGCGTTTT GCGT-Gwire2-T4 SEQ ID NO: 198 GGGGTTGGGGTTTTTTTGCGTTTT GCGT-Gwire2-T5 SEQ ID NO: 199 GGGGTTGGGGTTTTTTGCGTTTT GCGT-Gwire2-T6 SEQ ID NO: 200 GGGGTTGGGGTTTTTGCGTTTT GCGT-Gwire2- SEQ ID NO: 201 GGGGTTGGGGTTTTTTTTTTTGCGTTT eT1 GCGT-Gwire2- SEQ ID NO: 202 GGGGTTGGGGTTTTTTTTTTTGCGTT eT2 GCGT-Gwire2- SEQ ID NO: 203 GGGGTTGGGGTTTTTTTTTTTGCGT eT3 GCGT-Gwire3 SEQ ID NO: 224 GGGGTTGGGGTTGGGGTTTTTTTTTTTGCGTTTT GCGT-Gwire2-do SEQ ID NO: 204 GGGGTTGGGGTTTTTTTTTTTGCGTTTTGCGTTTT GCGT-Gwire2-tri SEQ ID NO: 205 GGGGTTGGGGTTTTTTTTTTTGCGTTTTGCGTTTTTGCGT TTT GCGA-Gwire2 SEQ ID NO: 177 GGGGTTGGGGTTTTTTTTTTTGCGATTT GCGA-Gwire2-do SEQ ID NO: 206 GGGGTTGGGGTTTTTTTTTTTGCGATTTGCGATTT GCGA-Gwire2-tri SEQ ID NO: 207 GGGGTTGGGGTTTTTTTTTTTGCGATTTGCGATTTGCGAT TT ACGC-Gwire2 SEQ ID NO: 184 GGGGTTGGGGTTTTTTTTTTTACGCTTT ACGC-Gwire2-do SEQ ID NO: 208 GGGGTTGGGGTTTTTTTTTTTACGCTTTACGCTTT ACGC-Gwire2-tri SEQ ID NO: 209 GGGGTTGGGGTTTTTTTTTTTACGCTTTACGCTTTACGCT TT TCGC-Gwire2 SEQ ID NO: 187 GGGGTTGGGGTTTTTTTTTTTTCGCTTT TCGC-Gwire2-do SEQ ID NO: 210 GGGGTTGGGGTTTTTTTTTTTTCGCTTTTCGCTTT TCGC-Gwire2-tri SEQ ID NO: 211 GGGGTTGGGGTTTTTTTTTTTTCGCTTTTCGCTTTTCGCT TT CCGC-Gwire2 SEQ ID NO: 186 GGGGTTGGGGTTTTTTTTTTTCCGCTTT CCGC-Gwire2-do SEQ ID NO: 212 GGGGTTGGGGTTTTTTTTTTTCCGCTTTCCGCTTT CCGC-Gwire2-tri SEQ ID NO: 213 GGGGTTGGGGTTTTTTTTTTTCCGCTTTCCGCTTTCCGCT TT GCGG-Gwire2-mo SEQ ID NO: 181 GGGGTTGGGGTTTTTTTTTTTGCGGTTT GCGG-Gwire2-do SEQ ID NO: 214 GGGGTTGGGGTTTTTTTTTTTGCGGTTTGCGGTTT GCGG-Gwire2-tri SEQ ID NO: 215 GGGGTTGGGGTTTTTTTTTTTGCGGTTTGCGGTTTGCGGT TT CG-Gw2-T0 SEQ ID NO: 216 GGGGTTGGGGTTTTTTTTCGCGCGTTT CG-Gw2-T1 SEQ ID NO: 217 GGGGTTGGGGTTTTTTTTCGTCGTCGTTT CG-Gw2-T2 SEQ ID NO: 218 GGGGTTGGGGTTTTTTTTCGTTCGTTCGTTT CG-Gw2-T3 SEQ ID NO: 219 GGGGTTGGGGTTTTTTTTCGTTTCGTTTCGTTT CG-Gw2-T4 SEQ ID NO: 220 GGGGTTGGGGTTTTTTTTCGTTTTCGTTTTCGTTT CG-Gw2-abase SEQ ID NO: 221 GGGGTTGGGGTTTTTTTTCGXCGXCGTTT X = abasic site CG-Gw2X1 SEQ ID NO: 222** GGGGTTGGGGTTTTTTTTCGX1CGX1CGTTT X1 = C18 CG-Gw2X2 SEQ ID NO: 223** GGGGTTGGGGTTTTTTTTCGX2CGX2CGTTT X2 = C3 CG-Gw2X2-1 SEQ ID NO: 225** GGGGTTGGGGTTTTTTTTCGX2CGTTT X2 = C3 CG-Gw2X2-2 SEQ ID NO: 223** GGGGTTGGGGTTTTTTTTCGX2CGX2CGTTT X2 = C3 CG-Gw2X2-3 SEQ ID NO: 226** GGGGTTGGGGTTTTTTTTCGX2CGX2CGX2CGTTT X2 = C3 CG-Gw2X2-4 SEQ ID NO: 227** GGGGTTGGGGTTTTTTTTCGX2CGX2CGX2CGX2CGTTT X2 = C3 CG-Gw2X2-5 SEQ ID NO: 228** GGGGTTGGGGTTTTTTTTCGX2CGX2CGX2CGX2CGX2CG TTT X2 = C3 CG-G4T16X2-1 SEQ ID NO: 229** TGGGGTTTTTTTTCGX2CGTTT X2 = C3 CG-G4T16X2-2 SEQ ID NO: 230** TGGGGTTTTTTTTCGX2CGX2CGTTT X2 = C3 CG-G4T16X2-3 SEQ ID NO: 231** TGGGGTTTTTTTTCGX2CGX2CGX2CGTTT X2 = C3 CG-G4T16X2-4 SEQ ID NO: 232** TGGGGTTTTTTTTCGX2CGX2CGX2CGX2CGTTT X2 = C3 CG-G4T16X2-5 SEQ ID NO: 233** TGGGGTTTTTTTTCGX2CGX2CGX2CGX2CGX2CGTTT X2 = C3 ODN-X2 SEQ ID NO: 234** GGGGTTGGGGTTTTTTTTCGX2CGX2CGTTT (X2 = Ethanediol) ODN-X3 SEQ ID NO: 223** GGGGTTGGGGTTTTTTTTCGX3CGX3CGTTT (X3 = Propanediol) ODN-X4 SEQ ID NO: 235** GGGGTTGGGGTTTTTTTTCGX4CGX4CGTTT (X4 =Butanediol) ODN-X6 SEQ ID NO: 236** GGGGTTGGGGTTTTTTTTCGX6CGX6CGTTT (X6 = Hexanediol ODN-X9 SEQ ID NO: 237** GGGGTTGGGGTTTTTTTTCGX9CGX9CGTTT (X9 = Nonanediol) ODN-X12 SEQ ID NO: 238** GGGGTTGGGGTTTTTTTTCGX12CGX12CGTTT (X12 = Dodecanediol) ODN-Xab SEQ ID NO: 239 GGGGTTGGGGTTTTTTTTCGXabCGXabCGTTT (Xab = dSpacer (abasic)) ODN-XtrEG SEQ ID NO: 240** GGGGTTGGGGTTTTTTTTCGXtrCGXtrCGTTT (Xtr = Triethyleneglycol) ACGC-Gw2X1 SEQ ID NO: 241** GGGGTTGGGGTTTTTTTTACGCX1ACGCX1ACGCTTT X1 = C18 (HEG*) CCGC-Gw2X1 SEQ ID NO: 242** GGGGTTGGGGTTTTTTTTCCGCX1CCGCX1CCGCTTT X1 = C18 (HEG*) ACGC-Gw2X2 SEQ ID NO: 243** GGGGTTGGGGTTTTTTTTACGCX2ACGCX2ACGCTTT X2 = Propanediol CCGC-Gw2X2 SEQ ID NO: 244** GGGGTTGGGGTTTTTTTTCCGCX2CCGCX2CCGCTTT X2 = Propanediol ACGC-G4T16-X2 SEQ ID NO: 245** TGGGGTTTTTTTTACGCX2ACGCX2ACGCTTT X2 = Propanediol CCGC-G4T16-X2 SEQ ID NO: 246** TGGGGTTTTTTTTCCGCX2CCGCX2CCGCTTT X2 = Propanediol 2006-PDE5dG4- SEQ ID NO: 247** GGGGX1TCGTCGTTTTGTCGTTTTGTCGTT X1 X1 = C18 (HEG*) 2006-PDE5dG4- SEQ ID NO: 248** GGGGX2TCGTCGTTTTGTCGTTTTGTCGTT X2 X2 = Propanediol 2006-PDE5dG4- SEQ ID NO: 249** GGGGX3GGGGTCGTCGTTTTGTCGTTTTGTCGTT X3 X3 = C18 (HEG*) 2006-PDE5dG4- SEQ ID NO: 250** GGGGX4GGGGTCGTCGTTTTGTCGTTTTGTCGTT X4 X4 = Propanediol 2006-T4-5dTG4T SEQ ID NO: 251 TGGGGTTTTTTCGTCGTTTTGTCGTTTTGTCGTT 2006-T4TG4T-3C SEQ ID NO: 251 TGGGGTTTTTTCGTCGTTTTGTCGTTTTGTCGTTX 3′-Cholesteryl 5Chol-GCGT3- SEQ ID NO: 1 XTGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT TG4T X = 5′-Cholesteryl GCGT3-TG4T SEQ ID NO: 252 TGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT GCGT-3-Gw2- SEQ ID NO: 253 XGGGGTTGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTT 5Chol TT 5′-Cholesteryl GCGT-3-Gw2 SEQ ID NO: 253 GGGGTTGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTT T GCGT3-5Chol SEQ ID NO: 254 XTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT X = 5′-Cholesteryl GCGT3 SEQ ID NO: 254 TTTTTTTGCGTTTTTGCGTTTTTGCGTTTT 5Chol-CCGC3- SEQ ID NO: 255 XGGGGTTGGGGTTTTTTTTCCGCTTTTCCGCTTTTCCGCT Gw2 TT X = 5′-Cholesteryl CCGC3-Gw2 SEQ ID NO: 255 GGGGTTGGGGTTTTTTTTCCGCTTTTCCGCTTTTCCGCTT T 5Chol-CCGC3 SEQ ID NO: 256 XTTTTTTTCCGCTTTTCCGCTTTTCCGCTTT X = 5′-Cholesteryl CCGC3 SEQ ID NO: 256 TTTTTTTCCGCTTTTCCGCTTTTCCGCTTT (lower case: PTO bonds, upper case PDE bonds) *Hexaethyleneglycol **As referred to herein, sequence names (e.g., “CG-Gw2X1,” etc.) refer to the full sequences shown in this table, including the X1, X2, X3, X4, X6, X9, X12,and Xtr non-nucleotide linkers.

The immunogenic nucleic acid plasmids described herein are enriched in CpG motifs. In some aspects, the immunogenic nucleic acid plasmids contain more than 20% CpG motifs compared to the frequency of CpG motifs found in vertebrate nucleic acid sequences.

In some aspects, the present disclosure relates to immunogenic nucleic acid plasmids that do not comprise an antibiotic resistance gene. In some aspects, the plasmids do not comprise a nucleic acid sequence coding for a full-length or functional selectable or screenable marker. For example, the pGCMB75.6 plasmid described herein does not comprise any full-length or functional selectable or screenable marker genes. The sequence of pGCMB75.6 is provided in SEQ ID NO:265 (Table 1A). In some aspects, the plasmids described herein do not encode an immunogen.

In some aspects, the immunogenic plasmids may comprise a nucleic acid sequence coding for a selectable or screenable marker gene that is not an antibiotic resistance gene. For example, the pLacZMB75.6 plasmid described herein comprises a LacZ gene as a screenable marker. The sequence of pLacZMB75.6 is provided in SEQ ID NO:268. In still other aspects, the plasmid will contain an antibiotic resistance gene. For example, pMB75.6 comprises a nucleic acid sequence encoding a resistance to the antibiotic kanamycin. The sequence of pMB75.6 is provided in SEQ ID NO:266.

It will be appreciated that the nucleotide sequence of the pMB75.6, pGCMB75.6, or pLacZMB75.6 plasmid may be varied to a certain extent without significantly adversely affecting its immunostimulatory properties. In some aspects are provided an immunogenic nucleic acid plasmids comprising or consisting of a nucleic acid sequence having at least 89% sequence identity with the sequence of pGCMB75.6 (SEQ ID NO: 265). In some aspects, the immunogenic plasmid comprises a nucleic acid sequence having at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity with the sequence of pGCMB75.6 (SEQ ID NO:265). In some aspects, the immunogenic nucleic acid plasmid comprises the sequence of pGCMB75.6 (SEQ ID NO:265).

In some aspects are provided immunogenic nucleic acid plasmids comprising a nucleic acid sequence having at least 84% sequence identity with the sequence of pLacZMB75.6 (SEQ ID NO:268). In some aspects, the immunogenic plasmid comprises or consists of a nucleic acid sequence having at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity with the sequence of pLacZMB75.6 (SEQ ID NO:268). In some aspects, the immunogenic nucleic acid comprises a plasmid having the sequence of pLacZMB75.6 (SEQ ID NO:268).

In some aspects are provided immunogenic nucleic acid plasmids comprising a nucleic acid sequence having at least 80% sequence identity with the sequence of SEQ ID NO:266. In some aspects, the immunogenic plasmid comprises or consists of a nucleic acid sequence having at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity with the sequence of SEQ ID NO:266. In some aspects, the immunogenic nucleic acid plasmid comprises the sequence of SEQ ID NO:266.

In some aspects are provided an immunogenic nucleic acid plasmid comprising a nucleic acid sequence having at least 80% sequence identity with the sequence of pMB75.6_AscI (SEQ ID NO:267). In some aspects, the immunogenic plasmid comprises or consists of a nucleic acid sequence having at least 75%, at least 76%, at least 77%, at least 78%, at least 79%, at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity with the sequence of SEQ ID NO:267. In some aspects, the immunogenic nucleic acid plasmid comprises the sequence of SEQ ID NO:267.

TABLE 1A Plasmid sequences pGCMB75.6 (SEQ ID NO: 265) tgaccgccca acgacccccg cccattgacg tcaataatga cgtatgttcc catagtaacg 60 ccaataggga ctttccattg acgtcaatgg gtggagtatt tacggtaaac tgcccacttg 120 gcagtacatc aagtgtatca tatgccaagt ccgcccccta ttgacgtcaa tgacggtaaa 180 tggcccgcct ggcattatgc ccagtacatg accttacggg actttcctac ttggcagtac 240 atctacgtat tagtcatcgc tattaccatg gtgatgcggt tttggcagta catcaatggg 300 cgtggatagc ggtttgactc acggggattt ccaagtctcc accccattga cgtcaatggg 360 agtttgtttt ggcaccaaaa tcaacgggac tttccaaaat gtcgtaacaa ctccgcccca 420 ttgacgcaaa tgggcggtag gcgtgtacgg tgggaggtct atataagcag agctcgttta 480 gtgaaccgtc agatcgcctg gagacgccat ccacgctgtt ttgacctcca tagaagacac 540 cgggaccgat ccagcctccc ctcgaagccg atctgataac ggtaccgata agctggcggc 600 cgattaagct acagaagttg gtcgtgaggc actgggcagg taagtatcaa ggttacaaga 660 caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact cttgcgtttc 720 tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac aggtgtccac 780 tcccaggttc aattacagct cttaagcagc cgcaagcttg atatcgaatt cctgcagccc 840 gggggatcca ctagttctag agcggccgcc accgcggtgg agctcgaatt atcagatcga 900 ttaataacta tgctcaaaaa ttgtgtacct ttagcttttt aatttgtaaa ggggttaata 960 aggaatattt gatgtatagt gccttgacta gagatcataa tcagccatac cacatttgta 1020 gaggttttac ttgctttaaa aaacctccca cacctccccc tgaacctgaa acataaaatg 1080 aatgcaattg ttgttgttaa cttgtttatt gcagcttata atggttacaa ataaagcaat 1140 agcatcacaa atttcacaaa taaagcattt ttttcactgc attctagttg tggtttgtcc 1200 aaactcatca atgtatctta tcatgtctgg atcatcagat ctgccggtct ccctatagtg 1260 agtcgtatta atttcgataa gccaggttaa cctgcattaa tgaatcggcc aacgcgcggg 1320 gagaggcggt ttgcgtattg ggcgctcttc cgcttcctcg ctcactgact cgctgcgctc 1380 ggtcgttcgg ctgcggcgag cggtatcagc tcactcaaag gcggtaatac ggttatccac 1440 agaatcaggg gataacgcag gaaagaacat gtgagcaaaa ggccagcaaa aggccaggaa 1500 ccgtaaaaag gccgcgttgc tggcgttttt ccataggctc cgcccccctg acgagcatca 1560 caaaaatcga cgctcaagtc agaggtggcg aaacccgaca ggactataaa gataccaggc 1620 gtttccccct ggaagctccc tcgtgcgctc tcctgttccg accctgccgc ttaccggata 1680 cctgtccgcc tttctccctt cgggaagcgt ggcgctttct catagctcac gctgtaggta 1740 tctcagttcg gtgtaggtcg ttcgctccaa gctgggctgt gtgcacgaac cccccgttca 1800 gcccgaccgc tgcgccttat ccggtaacta tcgtcttgag tccaacccgg taagacacga 1860 cttatcgcca ctggcagcag ccactggtaa caggattagc agagcgaggt atgtaggcgg 1920 tgctacagag ttcttgaagt ggtggcctaa ctacggctac actagaagaa cagtatttgg 1980 tatctgcgct ctgctgaagc cagttacctt cggaaaaaga gttggtagct cttgatccgg 2040 caaacaaacc accgctggta gcggtggttt ttttgtttgc aagcagcaga ttacgcgcag 2100 aaaaaaagga tctcaagaag atcctttgat cttttctacg gggtctgacg ctcagtggaa 2160 cgaaaactca cgttaaggga ttttggtcat gggcgcgcct aggcttttgc aaagatcgat 2220 caagagacag gatgaggatc gtttcgcagc ttttcattct gactgcaacg ggcaataagt 2280 ctctgtgtgg attaaaaaaa gagtgtctga tagcagcttc tgaactggtt acctgccgtg 2340 agtaaattaa aattttattg acttaggtca ctaaggcgcc ttgcgctgag gttgcgtcgt 2400 gatatcatca gggcagaccg gttacatccc cctaacaagc tgtataaaga gaaatactat 2460 ctcattggcg ttgcccgcac ctgacagtgc gacgttgggc tgcgtccgtc gaccaacggt 2520 accgaggtaa cagcccaatc tatccatgat ctcggccagg ccgggtcggc cgttatgcag 2580 cccggctcgg gtatgaagcc attaaggagc cgacccagcg cgaccgggcg gccggtcacg 2640 ctgcctctgc tgaagcctgc ctgtcactcc ctgcgcggcg tacccgccgt tctcatcgag 2700 taggctccgg atcgcgaccc cggacgggcc ctgggcccag gagcggccta tgacaaatgc 2760 cgggtagcga tccggcattc agcattgact gcgcacggat ccagtccttg caggagcctt 2820 atgccgaccg tagcaaaaaa tgagcccgag ccgatcgcga gttgtgatcc ggtcccgccg 2880 attgccggtc gcgatgacgg tcctgtgtaa gcgttatcgt taccaattgt ttaagaagta 2940 tatacgctac gaggtacttg ataacttctg cgtagcatac atgaggtttt gtataaaaat 3000 ggcgggcgat atcaacgcag tgtcagaaat ccgaaacagt ctgcgggact ctggggttcg 3060 aaatgaccga ccaagcgacg cccaacctgc catcacgaga tttcgattcc accgccgcct 3120 tctatgaaag gttgggcttc ggaatcgttt tccgggacgc cggctggatg atcctccagc 3180 gcggggatct catgctggag ttcttcgccc accctaggcg cgctcatgag cggatacata 3240 tttgaatgta tttagaaaaa taaacaaata ggggttccgc gcacatttcc ccgaaaagtg 3300 ccacctaaat tgtaagcgtt aatattttgt taaaattcgc gttaaatttt tgttaaatca 3360 gctcattttt taaccaatag gccgaaatcg gcaaaatccc ttataaatca aaagaataga 3420 ccgagatagg gttgagtgtt gttccagttt ggaacaagag tccactatta aagaacgtgg 3480 actccaacgt caaagggcga aaaaccgtct atcagggcga tggcccacta cgtgaaccat 3540 caccctaatc aagttttttg gggtcgaggt gccgtaaagc actaaatcgg aaccctaaag 3600 ggagcccccg atttagagct tgacggggaa agccggcgaa cgtggcgaga aaggaaggga 3660 agaaagcgaa aggagcgggc gctagggcgc tggcaagtgt agcggtcacg ctgcgcgtaa 3720 ccaccacacc cgccgcgctt aatgcgccgc tacagggcgc gtcccattcg ccattcaggc 3780 tgcgcaactg ttgggaaggg cgatcggtgc gggcctcttc gctattacgc cagctggcga 3840 aagggggatg tgctgcaagg cgattaagtt gggtaacgcc agggttttcc cagtcacgac 3900 gttgtaaaac gacggccagt gagcgcgcgt aatacgactc actatagggc gaattgggta 3960 ccgggccccc cctcgagcag gatctataca ttgaatcaat attggcaatt agccatatta 4020 gtcattggtt atatagcata aatcaatatt ggctattggc cattgcatac gttgtatcta 4080 tatcataata tgtacattta tattggctca tgtccaatat gaccgccatg ttgacattga 4140 ttattgacta gttattaata gtaatcaatt acggggtcat tagttcatag cccatatatg 4200 gagttccgcg ttacataact tacggtaaat ggcccgcctg gc 4242 pMB75.6 (SEQ ID NO: 266) ctaaattgta agcgttaata ttttgttaaa attcgcgtta aatttttgtt aaatcagctc 60 attttttaac caataggccg aaatcggcaa aatcccttat aaatcaaaag aatagaccga 120 gatagggttg agtgttgttc cagtttggaa caagagtcca ctattaaaga acgtggactc 180 caacgtcaaa gggcgaaaaa ccgtctatca gggcgatggc ccactacgtg aaccatcacc 240 ctaatcaagt tttttggggt cgaggtgccg taaagcacta aatcggaacc ctaaagggag 300 cccccgattt agagcttgac ggggaaagcc ggcgaacgtg gcgagaaagg aagggaagaa 360 agcgaaagga gcgggcgcta gggcgctggc aagtgtagcg gtcacgctgc gcgtaaccac 420 cacacccgcc gcgcttaatg cgccgctaca gggcgcgtcc cattcgccat tcaggctgcg 480 caactgttgg gaagggcgat cggtgcgggc ctcttcgcta ttacgccagc tggcgaaagg 540 gggatgtgct gcaaggcgat taagttgggt aacgccaggg ttttcccagt cacgacgttg 600 taaaacgacg gccagtgagc gcgcgtaata cgactcacta tagggcgaat tgggtaccgg 660 gccccccctc gagcaggatc tatacattga atcaatattg gcaattagcc atattagtca 720 ttggttatat agcataaatc aatattggct attggccatt gcatacgttg tatctatatc 780 ataatatgta catttatatt ggctcatgtc caatatgacc gccatgttga cattgattat 840 tgactagtta ttaatagtaa tcaattacgg ggtcattagt tcatagccca tatatggagt 900 tccgcgttac ataacttacg gtaaatggcc cgcctggctg accgcccaac gacccccgcc 960 cattgacgtc aataatgacg tatgttccca tagtaacgcc aatagggact ttccattgac 1020 gtcaatgggt ggagtattta cggtaaactg cccacttggc agtacatcaa gtgtatcata 1080 tgccaagtcc gccccctatt gacgtcaatg acggtaaatg gcccgcctgg cattatgccc 1140 agtacatgac cttacgggac tttcctactt ggcagtacat ctacgtatta gtcatcgcta 1200 ttaccatggt gatgcggttt tggcagtaca tcaatgggcg tggatagcgg tttgactcac 1260 ggggatttcc aagtctccac cccattgacg tcaatgggag tttgttttgg caccaaaatc 1320 aacgggactt tccaaaatgt cgtaacaact ccgccccatt gacgcaaatg ggcggtaggc 1380 gtgtacggtg ggaggtctat ataagcagag ctcgtttagt gaaccgtcag atcgcctgga 1440 gacgccatcc acgctgtttt gacctccata gaagacaccg ggaccgatcc agcctcccct 1500 cgaagccgat ctgataacgg taccgataag ctggcggccg attaagctac agaagttggt 1560 cgtgaggcac tgggcaggta agtatcaagg ttacaagaca ggtttaagga gaccaataga 1620 aactgggctt gtcgagacag agaagactct tgcgtttctg ataggcacct attggtctta 1680 ctgacatcca ctttgccttt ctctccacag gtgtccactc ccaggttcaa ttacagctct 1740 taagcagccg caagcttgat atcgaattcc tgcagcccgg gggatccact agttctagag 1800 cggccgccac cgcggtggag ctcgaattat cagatcgatt aataactatg ctcaaaaatt 1860 gtgtaccttt agctttttaa tttgtaaagg ggttaataag gaatatttga tgtatagtgc 1920 cttgactaga gatcataatc agccatacca catttgtaga ggttttactt gctttaaaaa 1980 acctcccaca cctccccctg aacctgaaac ataaaatgaa tgcaattgtt gttgttaact 2040 tgtttattgc agcttataat ggttacaaat aaagcaatag catcacaaat ttcacaaata 2100 aagcattttt ttcactgcat tctagttgtg gtttgtccaa actcatcaat gtatcttatc 2160 atgtctggat catcagatct gccggtctcc ctatagtgag tcgtattaat ttcgataagc 2220 caggttaacc tgcattaatg aatcggccaa cgcgcgggga gaggcggttt gcgtattggg 2280 cgctcttccg cttcctcgct cactgactcg ctgcgctcgg tcgttcggct gcggcgagcg 2340 gtatcagctc actcaaaggc ggtaatacgg ttatccacag aatcagggga taacgcagga 2400 aagaacatgt gagcaaaagg ccagcaaaag gccaggaacc gtaaaaaggc cgcgttgctg 2460 gcgtttttcc ataggctccg cccccctgac gagcatcaca aaaatcgacg ctcaagtcag 2520 aggtggcgaa acccgacagg actataaaga taccaggcgt ttccccctgg aagctccctc 2580 gtgcgctctc ctgttccgac cctgccgctt accggatacc tgtccgcctt tctcccttcg 2640 ggaagcgtgg cgctttctca tagctcacgc tgtaggtatc tcagttcggt gtaggtcgtt 2700 cgctccaagc tgggctgtgt gcacgaaccc cccgttcagc ccgaccgctg cgccttatcc 2760 ggtaactatc gtcttgagtc caacccggta agacacgact tatcgccact ggcagcagcc 2820 actggtaaca ggattagcag agcgaggtat gtaggcggtg ctacagagtt cttgaagtgg 2880 tggcctaact acggctacac tagaagaaca gtatttggta tctgcgctct gctgaagcca 2940 gttaccttcg gaaaaagagt tggtagctct tgatccggca aacaaaccac cgctggtagc 3000 ggtggttttt ttgtttgcaa gcagcagatt acgcgcagaa aaaaaggatc tcaagaagat 3060 cctttgatct tttctacggg gtctgacgct cagtggaacg aaaactcacg ttaagggatt 3120 ttggtcatga gcgcgcctag gcttttgcaa agatcgatca agagacagga tgaggatcgt 3180 ttcgcatgat tgaacaagat ggattgcacg caggttctcc ggccgcttgg gtggagaggc 3240 tattcggcta tgactgggca caacagacaa tcggctgctc tgatgccgcc gtgttccggc 3300 tgtcagcgca ggggcgcccg gttctttttg tcaagaccga cctgtccggt gccctgaatg 3360 aactgcaaga cgaggcagcg cggctatcgt ggctggccac gacgggcgtt ccttgcgcag 3420 ctgtgctcga cgttgtcact gaagcgggaa gggactggct gctattgggc gaagtgccgg 3480 ggcaggatct cctgtcatct caccttgctc ctgccgagaa agtatccatc atggctgatg 3540 caatgcggcg gctgcatacg cttgatccgg ctacctgccc attcgaccac caagcgaaac 3600 atcgcatcga gcgagcacgt actcggatgg aagccggtct tgtcgatcag gatgatctgg 3660 acgaagagca tcaggggctc gcgccagccg aactgttcgc caggctcaag gcgagcatgc 3720 ccgacggcga ggatctcgtc gtgacccatg gcgatgcctg cttgccgaat atcatggtgg 3780 aaaatggccg cttttctgga ttcatcgact gtggccggct gggtgtggcg gaccgctatc 3840 aggacatagc gttggctacc cgtgatattg ctgaagagct tggcggcgaa tgggctgacc 3900 gcttcctcgt gctttacggt atcgccgctc ccgattcgca gcgcatcgcc ttctatcgcc 3960 ttcttgacga gttcttctga gcgggactct ggggttcgaa atgaccgacc aagcgacgcc 4020 caacctgcca tcacgagatt tcgattccac cgccgccttc tatgaaaggt tgggcttcgg 4080 aatcgttttc cgggacgccg gctggatgat cctccagcgc ggggatctca tgctggagtt 4140 cttcgcccac cctaggcgcg ctcatgagcg gatacatatt tgaatgtatt tagaaaaata 4200 aacaaatagg ggttccgcgc acatttcccc gaaaagtgcc ac 4242 pMB75.6_AscI (SEQ ID NO: 267) tgaccgccca acgacccccg cccattgacg tcaataatga cgtatgttcc catagtaacg 60 ccaataggga ctttccattg acgtcaatgg gtggagtatt tacggtaaac tgcccacttg 120 gcagtacatc aagtgtatca tatgccaagt ccgcccccta ttgacgtcaa tgacggtaaa 180 tggcccgcct ggcattatgc ccagtacatg accttacggg actttcctac ttggcagtac 240 atctacgtat tagtcatcgc tattaccatg gtgatgcggt tttggcagta catcaatggg 300 cgtggatagc ggtttgactc acggggattt ccaagtctcc accccattga cgtcaatggg 360 agtttgtttt ggcaccaaaa tcaacgggac tttccaaaat gtcgtaacaa ctccgcccca 420 ttgacgcaaa tgggcggtag gcgtgtacgg tgggaggtct atataagcag agctcgttta 480 gtgaaccgtc agatcgcctg gagacgccat ccacgctgtt ttgacctcca tagaagacac 540 cgggaccgat ccagcctccc ctcgaagccg atctgataac ggtaccgata agctggcggc 600 cgattaagct acagaagttg gtcgtgaggc actgggcagg taagtatcaa ggttacaaga 660 caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact cttgcgtttc 720 tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac aggtgtccac 780 tcccaggttc aattacagct cttaagcagc cgcaagcttg atatcgaatt cctgcagccc 840 gggggatcca ctagttctag agcggccgcc accgcggtgg agctcgaatt atcagatcga 900 ttaataacta tgctcaaaaa ttgtgtacct ttagcttttt aatttgtaaa ggggttaata 960 aggaatattt gatgtatagt gccttgacta gagatcataa tcagccatac cacatttgta 1020 gaggttttac ttgctttaaa aaacctccca cacctccccc tgaacctgaa acataaaatg 1080 aatgcaattg ttgttgttaa cttgtttatt gcagcttata atggttacaa ataaagcaat 1140 agcatcacaa atttcacaaa taaagcattt ttttcactgc attctagttg tggtttgtcc 1200 aaactcatca atgtatctta tcatgtctgg atcatcagat ctgccggtct ccctatagtg 1260 agtcgtatta atttcgataa gccaggttaa cctgcattaa tgaatcggcc aacgcgcggg 1320 gagaggcggt ttgcgtattg ggcgctcttc cgcttcctcg ctcactgact cgctgcgctc 1380 ggtcgttcgg ctgcggcgag cggtatcagc tcactcaaag gcggtaatac ggttatccac 1440 agaatcaggg gataacgcag gaaagaacat gtgagcaaaa ggccagcaaa aggccaggaa 1500 ccgtaaaaag gccgcgttgc tggcgttttt ccataggctc cgcccccctg acgagcatca 1560 caaaaatcga cgctcaagtc agaggtggcg aaacccgaca ggactataaa gataccaggc 1620 gtttccccct ggaagctccc tcgtgcgctc tcctgttccg accctgccgc ttaccggata 1680 cctgtccgcc tttctccctt cgggaagcgt ggcgctttct catagctcac gctgtaggta 1740 tctcagttcg gtgtaggtcg ttcgctccaa gctgggctgt gtgcacgaac cccccgttca 1800 gcccgaccgc tgcgccttat ccggtaacta tcgtcttgag tccaacccgg taagacacga 1860 cttatcgcca ctggcagcag ccactggtaa caggattagc agagcgaggt atgtaggcgg 1920 tgctacagag ttcttgaagt ggtggcctaa ctacggctac actagaagaa cagtatttgg 1980 tatctgcgct ctgctgaagc cagttacctt cggaaaaaga gttggtagct cttgatccgg 2040 caaacaaacc accgctggta gcggtggttt ttttgtttgc aagcagcaga ttacgcgcag 2100 aaaaaaagga tctcaagaag atcctttgat cttttctacg gggtctgacg ctcagtggaa 2160 cgaaaactca cgttaaggga ttttggtcat gggcgcgcct aggcttttgc aaagatcgat 2220 caagagacag gatgaggatc gtttcgcatg attgaacaag atggattgca cgcaggttct 2280 ccggccgctt gggtggagag gctattcggc tatgactggg cacaacagac aatcggctgc 2340 tctgatgccg ccgtgttccg gctgtcagcg caggggcgcc cggttctttt tgtcaagacc 2400 gacctgtccg gtgccctgaa tgaactgcaa gacgaggcag cgcggctatc gtggctggcc 2460 acgacgggcg ttccttgcgc agctgtgctc gacgttgtca ctgaagcggg aagggactgg 2520 ctgctattgg gcgaagtgcc ggggcaggat ctcctgtcat ctcaccttgc tcctgccgag 2580 aaagtatcca tcatggctga tgcaatgcgg cggctgcata cgcttgatcc ggctacctgc 2640 ccattcgacc accaagcgaa acatcgcatc gagcgagcac gtactcggat ggaagccggt 2700 cttgtcgatc aggatgatct ggacgaagag catcaggggc tcgcgccagc cgaactgttc 2760 gccaggctca aggcgagcat gcccgacggc gaggatctcg tcgtgaccca tggcgatgcc 2820 tgcttgccga atatcatggt ggaaaatggc cgcttttctg gattcatcga ctgtggccgg 2880 ctgggtgtgg cggaccgcta tcaggacata gcgttggcta cccgtgatat tgctgaagag 2940 cttggcggcg aatgggctga ccgcttcctc gtgctttacg gtatcgccgc tcccgattcg 3000 cagcgcatcg ccttctatcg ccttcttgac gagttcttct gagcgggact ctggggttcg 3060 aaatgaccga ccaagcgacg cccaacctgc catcacgaga tttcgattcc accgccgcct 3120 tctatgaaag gttgggcttc ggaatcgttt tccgggacgc cggctggatg atcctccagc 3180 gcggggatct catgctggag ttcttcgccc accctaggcg cgctcatgag cggatacata 3240 tttgaatgta tttagaaaaa taaacaaata ggggttccgc gcacatttcc ccgaaaagtg 3300 ccacctaaat tgtaagcgtt aatattttgt taaaattcgc gttaaatttt tgttaaatca 3360 gctcattttt taaccaatag gccgaaatcg gcaaaatccc ttataaatca aaagaataga 3420 ccgagatagg gttgagtgtt gttccagttt ggaacaagag tccactatta aagaacgtgg 3480 actccaacgt caaagggcga aaaaccgtct atcagggcga tggcccacta cgtgaaccat 3540 caccctaatc aagttttttg gggtcgaggt gccgtaaagc actaaatcgg aaccctaaag 3600 ggagcccccg atttagagct tgacggggaa agccggcgaa cgtggcgaga aaggaaggga 3660 agaaagcgaa aggagcgggc gctagggcgc tggcaagtgt agcggtcacg ctgcgcgtaa 3720 ccaccacacc cgccgcgctt aatgcgccgc tacagggcgc gtcccattcg ccattcaggc 3780 tgcgcaactg ttgggaaggg cgatcggtgc gggcctcttc gctattacgc cagctggcga 3840 aagggggatg tgctgcaagg cgattaagtt gggtaacgcc agggttttcc cagtcacgac 3900 gttgtaaaac gacggccagt gagcgcgcgt aatacgactc actatagggc gaattgggta 3960 ccgggccccc cctcgagcag gatctataca ttgaatcaat attggcaatt agccatatta 4020 gtcattggtt atatagcata aatcaatatt ggctattggc cattgcatac gttgtatcta 4080 tatcataata tgtacattta tattggctca tgtccaatat gaccgccatg ttgacattga 4140 ttattgacta gttattaata gtaatcaatt acggggtcat tagttcatag cccatatatg 4200 gagttccgcg ttacataact tacggtaaat ggcccgcctg gc 4242 pLacZMB75.6 (SEQ ID NO: 268) tgaccgccca acgacccccg cccattgacg tcaataatga cgtatgttcc catagtaacg 60 ccaataggga ctttccattg acgtcaatgg gtggagtatt tacggtaaac tgcccacttg 120 gcagtacatc aagtgtatca tatgccaagt ccgcccccta ttgacgtcaa tgacggtaaa 180 tggcccgcct ggcattatgc ccagtacatg accttacggg actttcctac ttggcagtac 240 atctacgtat tagtcatcgc tattaccatg gtgatgcggt tttggcagta catcaatggg 300 cgtggatagc ggtttgactc acggggattt ccaagtctcc accccattga cgtcaatggg 360 agtttgtttt ggcaccaaaa tcaacgggac tttccaaaat gtcgtaacaa ctccgcccca 420 ttgacgcaaa tgggcggtag gcgtgtacgg tgggaggtct atataagcag agctcgttta 480 gtgaaccgtc agatcgcctg gagacgccat ccacgctgtt ttgacctcca tagaagacac 540 cgggaccgat ccagcctccc ctcgaagccg atctgataac ggtaccgata agctggcggc 600 cgattaagct acagaagttg gtcgtgaggc actgggcagg taagtatcaa ggttacaaga 660 caggtttaag gagaccaata gaaactgggc ttgtcgagac agagaagact cttgcgtttc 720 tgataggcac ctattggtct tactgacatc cactttgcct ttctctccac aggtgtccac 780 tcccaggttc aattacagct cttaagcagc cgccaaaaca aaattcctca aaaatcatca 840 tcgaatgaat ggtgaaataa tttccctgaa taactgtagt gttttcaggg cgcggcataa 900 taattaacta tgctcaaaaa ttgtgtacct ttagcttttt aatttgtaaa ggggttaata 960 aggaatattt gatgtatagt gccttgacta gagatcataa tcagccatac cacatttgta 1020 gaggttttac ttgctttaaa aaacctccca cacctccccc tgaacctgaa acataaaatg 1080 aatgcaattg ttgttgttaa cttgtttatt gcagcttata atggttacaa ataaagcaat 1140 agcatcacaa atttcacaaa taaagcattt ttttcactgc attctagttg tggtttgtcc 1200 aaactcatca atgtatctta tcatgtctgg atcatcagat ctgccggtct ccctatagtg 1260 agtcgtatta atttcgataa gccaggttaa cctgcattaa tgaatcggcc aacgcgcggg 1320 gagaggcggt ttgcgtattg ggcgctcttc cgcttcctcg ctcactgact cgctgcgctc 1380 ggtcgttcgg ctgcggcgag cggtatcagc tcactcaaag gcggtaatac ggttatccac 1440 agaatcaggg gataacgcag gaaagaacat gtgagcaaaa ggccagcaaa aggccaggaa 1500 ccgtaaaaag gccgcgttgc tggcgttttt ccataggctc cgcccccctg acgagcatca 1560 caaaaatcga cgctcaagtc agaggtggcg aaacccgaca ggactataaa gataccaggc 1620 gtttccccct ggaagctccc tcgtgcgctc tcctgttccg accctgccgc ttaccggata 1680 cctgtccgcc tttctccctt cgggaagcgt ggcgctttct catagctcac gctgtaggta 1740 tctcagttcg gtgtaggtcg ttcgctccaa gctgggctgt gtgcacgaac cccccgttca 1800 gcccgaccgc tgcgccttat ccggtaacta tcgtcttgag tccaacccgg taagacacga 1860 cttatcgcca ctggcagcag ccactggtaa caggattagc agagcgaggt atgtaggcgg 1920 tgctacagag ttcttgaagt ggtggcctaa ctacggctac actagaagaa cagtatttgg 1980 tatctgcgct ctgctgaagc cagttacctt cggaaaaaga gttggtagct cttgatccgg 2040 caaacaaacc accgctggta gcggtggttt ttttgtttgc aagcagcaga ttacgcgcag 2100 aaaaaaagga tctcaagaag atcctttgat cttttctacg gggtctgacg ctcagtggaa 2160 cgaaaactca cgttaaggga ttttggtcat gggcgcgcct aggcttttgc aaagatcgat 2220 caagagacag gatgaggatc gtttcgcagc ttttcattct gactgcaacg ggcaataagt 2280 ctctgtgtgg attaaaaaaa gagtgtctga tagcagcttc tgaactggtt acctgccgtg 2340 agtaaattaa aattttattg acttaggtca ctaaggcgcc ttgcgctgag gttgcgtcgt 2400 gatatcatca gggcagaccg gttacatccc cctaacaagc tgtataaaga gaaatactat 2460 ctcattggcg ttgcccgcac ctgacagtgc gacgttgggc tgcgtccgtc gaccaacggt 2520 accgaggtaa cagcccaatc tatccatgat ctcggccagg ccgggtcggc cgttatgcag 2580 cccggctcgg gtatgaagcc attaaggagc cgacccagcg cgaccgggcg gccggtcacg 2640 ctgcctctgc tgaagcctgc ctgtcactcc ctgcgcggcg tacccgccgt tctcatcgag 2700 taggctccgg atcgcgaccc cggacgggcc ctgggcccag gagcggccta tgacaaatgc 2760 cgggtagcga tccggcattc agcattgact gcgcacggat ccagtccttg caggagcctt 2820 atgccgaccg tagcaaaaaa tgagcccgag ccgatcgcga gttgtgatcc ggtcccgccg 2880 attgccggtc gcgatgacgg tcctgtgtaa gcgttatcgt taccaattgt ttaagaagta 2940 tatacgctac gaggtacttg ataacttctg cgtagcatac atgaggtttt gtataaaaat 3000 ggcgggcgat atcaacgcag tgtcagaaat ccgaaacagt ctgcgggact ctggggttcg 3060 aaatgaccga ccaagcgacg cccaacctgc catcacgaga tttcgattcc accgccgcct 3120 tctatgaaag gttgggcttc ggaatcgttt tccgggacgc cggctggatg atcctccagc 3180 gcggggatct catgctggag ttcttcgccc accctaggcg cgctcatgag cggatacata 3240 tttgaatgta tttagaaaaa taaacaaata ggggttccgc gcacatttcc ccgaaaagtg 3300 ccacctaaat tgtaagcgtt aatattttgt taaaattcgc gttaaatttt tgttaaatca 3360 gctcattttt taaccaatag gccgaaatcg gcaaaatccc ttataaatca aaagaataga 3420 ccgagatagg gttgagtgtt gttccagttt ggaacaagag tccactatta aagaacgtgg 3480 actccaacgt caaagggcga aaaaccgtct atcagggcga tggcccacta cgtgaaccat 3540 caccctaatc aagttttttg gggtcgaggt gccgtaaagc actaaatcgg aaccctaaag 3600 ggagcccccg atttagagct tgacggggaa agccggcgaa cgtggcgaga aaggaaggga 3660 agaaagcgaa aggagcgggc gctagggcgc tggcaagtgt agcggtcacg ctgcgcgtaa 3720 ccaccacacc cgccgcgctt aatgcgccgc tacagggcgc gtcccattcg ccattcaggc 3780 tgcgcaactg ttgggaaggg cgatcggtgc gggcctcttc gctattacgc cagctggcga 3840 aagggggatg tgctgcaagg cgattaagtt gggtaacgcc agggttttcc cagtcacgac 3900 gttgtaaaac gacggccagt gagcgcgcgt aatacgactc actatagggc gaattgggta 3960 ccgggccccc cctcgaggtc gacggtatcg ataagcttga tatcgaattc ctgcagcccg 4020 ggggatccac tagttctaga gcggccgcca ccgcggtgga gctccagctt ttgttccctt 4080 tagtgagggt taattgcgcg cttggcgtaa tcatggtcat agctgtttcc tgtgtgaaat 4140 tgttatccgc tcacaattcc acacaacata cgagccggaa gcataaagtg taaagcctgg 4200 ggtgcctaat gagtgagcta actcacatta attgcgttgc gc 4242

Further provided herein are immunogenic nucleic acids or immunogenic plasmids capable of stimulating an immune response including nucleic acid sequences that hybridize under high stringency conditions to SEQ ID NO:265, SEQ ID NO:266, SEQ ID NO:267, or SEQ ID NO:268. Suitable nucleic acid sequences include those that are homologous, substantially similar, or identical to the nucleic acids described herein. In some aspects, homologous nucleic acid sequences will have a percent identity of at least about 75%, 76%, 77%, 78%, 79%, 80% 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% to SEQ ID NO:265 or the respective complementary sequence. In other aspects, homologous nucleic acid sequences will have a sequence similarity of at least about 75%, 76%, 77%, 78%, 79%, 80% 81%, 82%, 83%, 84%, 85%, 86%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% to SEQ ID NO:268 or the respective complementary sequence. In other aspects, homologous nucleic acid sequences will have a sequence similarity of at least about 75%, 76%, 77%, 78%, 79%, 80% 81%, 82%, 83%, 84%, 85%, 86%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% to SEQ ID NO:266 or the respective complementary sequence. In other aspects, homologous nucleic acid sequences will have a sequence similarity of at least about 75%, 76%, 77%, 78%, 79%, 80% 81%, 82%, 83%, 84%, 85%, 86%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% to SEQ ID NO:267 or the respective complementary sequence. Sequence similarity may be calculated using a number of algorithms known in the art, such as BLAST, described in Altschul, S. F., et al., J. Mol. Biol. 215:403-10, 1990. The nucleic acids may differ in sequence from the above-described nucleic acids due to the degeneracy of the genetic code. In general, a reference sequence will be 18 nucleotides, more usually 30 or more nucleotides, and may comprise the entire nucleic acid sequence of the composition for comparison purposes.

Nucleic acids that can hybridize to SEQ ID NO:265, SEQ ID NO:266, SEQ ID NO:267, or SEQ ID NO:268 are contemplated herein. Stringent hybridization conditions include conditions such as hybridization at 50° C. or higher and 0.1×SSC (15 mM sodium chloride/1.5 mM sodium citrate). Another example is overnight incubation at 42° C. in a solution of 50% formamide, 5×SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulfate, and 20 μg/ml denatured, sheared salmon sperm DNA, followed by washing in 0.1×SSC at about 65° C. Exemplary stringent hybridization conditions are hybridization conditions that are at least about 80%, 85%, 90%, or 95% as stringent as the above specific conditions. Other stringent hybridization conditions are known in the art and may also be employed to identify homologs of the nucleic acids of the present disclosure (Current Protocols in Molecular Biology, Unit 6, pub. John Wiley & Sons, N.Y. 1989).

It will be appreciated that the nucleotide sequences of the immunogenic nucleic acid plasmids may be varied to a certain extent without significantly adversely affecting their immunogenic properties. The nucleic acid sequence of such a variant nucleic acid plasmid molecule will usually differ by one or more nucleotides. The sequence changes may be substitutions, insertions, deletions, or a combination thereof. Techniques for mutagenesis of cloned genes are known in the art. Methods for site specific mutagenesis may be found in Gustin et al., Biotechniques 14:22, 1993; Barany, Gene 37:111-23, 1985; Colicelli et al., Mol. Gen. Genet. 199:537-9, 1985; and Sambrook et al., Molecular Cloning: A Laboratory Manual, CSH Press 1989, pp. 15.3-15.108 and all incorporated herein by reference. In summary, the invention relates to nucleic acid plasmid molecules, and variants or mutants thereof, capable of stimulating an innate immune response in a subject. Also, the invention encompasses the intermediary RNAs encoded by the described nucleic acids, as well as any resultant amino acid sequences encoded by the nucleic acid plasmids described herein.

In some aspects, where the nucleotide sequence of the immunogenic nucleic acid plasmid varies from the sequence provided in SEQ ID NOs:265, 266, 267, or 268, the CpG dinucleotides in the immunogenic nucleic acid plasmid are preferably left intact. Alternatively, if the nucleotide sequence of the immunogenic plasmid is altered such that a CpG dinucleotide is eliminated, the sequence of the immunogenic nucleic acid plasmid may be altered at another location such that the total number of CpG dinucleotides in the nucleic acid plasmid remains the same. Further CpG dinucleotides in addition to those already present in the immunogenic nucleic acid plasmid may also be introduced. Thus, for example, the immunogenic nucleic acid plasmids described herein comprise at least about 200, at least about 220, at least about 240, at least about 260, at least about 270, at least about 275, at least about 280, at least about 283, at least about 285, or at least about 288 CpG dinucleotides. In some embodiments, the immunogenic nucleic acid plasmid can comprise 283 CpG dinucleotides. In some embodiments, CpG dinucleotides in addition to those already present in the nucleotide sequences of pGCMB75.6 or pLacZMB75.6 are introduced into the plasmid.

In some aspects, where the nucleotide sequence of the immunogenic nucleic acid plasmid varies from the sequences provided herein, the CpG motif types in the immunogenic nucleic acid are varied to modulate the resultant activation of a cytosolic nucleic acid surveillance molecule, i.e., TLR21 and/or TLR9. For example, the number of immune stimulatory CpG motifs may be increased to enhance the activation of at least one cytosolic nucleic acid surveillance molecule responsive to an immunogenic nucleic acid plasmid. Alternatively, the number of non-immune stimulatory CpG motifs may be increased to reduce the activation of at least one cytosolic nucleic acid surveillance molecule. In some aspects, the number of stimulatory and nonstimulatory CpG motifs can be modified to enhance the activation of at least one cytosolic nucleic acid surveillance molecule and reduce the activation of at least one cytosolic nucleic acid surveillance molecule.

A suitable immunogenic nucleic acid plasmid molecule includes any of the immunogenic coding and noncoding nucleic acids described herein. Coding nucleic acid sequences encode at least a portion of a protein or peptide, while non-coding sequence does not encode any portion of a protein or peptide. According to the present invention, “non-coding” nucleic acids can include regulatory regions of a transcription unit, such as a promoter region. The term, “empty vector” can be used interchangeably with the term “non-coding,” and particularly refers to a nucleic acid sequence in the absence of a protein coding portion, such as a plasmid vector without a gene insert. Expression of a protein encoded by the nucleic acid plasmids described herein is not required for inducing an immune response; therefore, the plasmids need not contain any coding sequences operatively linked to a transcription control sequence. However, further advantages may be obtained (i.e., antigen-specific and enhanced immunity) by including in the immunomodulatory composition at least one nucleic acid sequence (DNA or RNA) which encodes an immunogen and/or a cytokine. Such a nucleic acid sequence encoding an immunogen and/or a cytokine may be included in the immunogenic nucleic acid plasmids described herein, or may be included in a separate nucleic acid (e.g., a separate plasmid) in the composition.

In some embodiments of the immunomodulatory compositions described herein, the immunomodulatory composition comprises a liposomal delivery vehicle and at least one of the immunogenic nucleic acid plasmids described herein. Suitable immunomodulatory compositions are described in U.S. Patent Application Publications Nos. 2012/0064151 A1 and 2013/0295167 A1, the contents of both are hereby incorporated by reference in their entirety.

A suitable liposomal delivery vehicle comprises a lipid composition that is capable of delivering nucleic acid molecules to the tissues of a treated subject. In some embodiments, a liposomal delivery vehicle may be capable of remaining stable in a subject for a sufficient amount of time to deliver a nucleic acid molecule and/or a biological agent. For example, the liposomal delivery vehicle is stable in the recipient subject for at least about five minutes, for at least about 1 hour, or for at least about 24 hours.

A liposomal delivery vehicle as described herein comprises a lipid composition that is capable of fusing with the plasma membrane of a cell to deliver a nucleic acid molecule into a cell. When the nucleic acid molecule encodes one or more proteins, the nucleic acid:liposome complex has, in some aspects, a transfection efficiency of at least about 1 picogram (pg) of protein expressed per milligram (mg) of total tissue protein per microgram (μg) of nucleic acid delivered. For example, the transfection efficiency of a nucleic acid: liposome complex can be at least about 10 pg of protein expressed per mg of total tissue protein per μg of nucleic acid delivered; or at least about 50 pg of protein expressed per mg of total tissue protein per μg of nucleic acid delivered. The transfection efficiency of the complex may be as low as 1 femtogram (fg) of protein expressed per mg of total tissue protein per μg of nucleic acid delivered, with the above amounts being more preferred.

In some embodiments, the liposomal delivery vehicle of the present invention is between about 100 and 500 nanometers (nm) in diameter. For example, the liposomal delivery vehicle can be between about 150 and 450 nm or between about 200 and 400 nm in diameter.

Suitable liposomes include any liposome, such as those commonly used in, for example, gene delivery methods known to those of skill in the art. In some embodiments, liposomal delivery vehicles comprise multilamellar vesicle (MLV) lipids, extruded lipids, or both. In some aspects, the liposomal delivery vehicle is cationic. Methods for preparation of MLVs are well known in the art. In some aspects, liposomal delivery vehicles comprise liposomes having a polycationic lipid composition (i.e., cationic liposomes) and/or liposomes having a cholesterol backbone conjugated to polyethylene glycol. Exemplary cationic liposome compositions include, but are not limited to, N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) and cholesterol, N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTAP) and cholesterol, 1-[2-(oleoyloxy)ethyl]-2-oleyl-3-(2-hydroxyethyl)-imidazolinium chloride (DOTIM) and cholesterol, dimethyldioctadecylammonium bromide (DDAB) and cholesterol, and combinations thereof. In some aspects, the liposomal delivery vehicle comprises pairs of lipids selected from the group consisting of N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) and cholesterol; N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTAP) and cholesterol; 1-[2-(oleoyloxy)ethyl]-2-oleyl-3-(2-hydroxyethyl)imidazolinium chloride (DOTIM) and cholesterol; and dimethyldioctadecylammonium bromide (DDAB) and cholesterol. In some aspects, the liposome composition for use as a delivery vehicle includes DOTIM and cholesterol.

Complexing a liposome with a herein described immunogenic nucleic acid plasmid may be achieved using methods standard in the art or as described in U.S. Pat. No. 6,693,086, the contents of which are hereby incorporated by reference in their entirety. A suitable concentration of nucleic acid plasmid to add to a liposome includes a concentration effective for delivering a sufficient amount of the immunogenic nucleic acid plasmid into a subject such that a systemic immune response is elicited. For example, from about 0.1 μg to about 10 μg of immunogenic nucleic acid plasmid can be combined with about 8 nmol liposomes, from about 0.5 μg to about 5 μg of immunogenic nucleic acid plasmid can be combined with about 8 nmol liposomes, or about 1.0 μg of immunogenic nucleic acid plasmid can be combined with about 8 nmol liposomes. The ratio of immunogenic nucleic acid plasmid to lipid (μg immunogenic nucleic acid plasmid:nmol lipid) in a composition can be at least about 1:1 immunogenic nucleic acid plasmid:lipid by weight (e.g., 1 μg immunogenic nucleic acid plasmid:1 nmol lipid). For example, the ratio of immunogenic nucleic acid plasmid to lipids can be at least about 1:5, at least about 1:10, or at least about 1:20. Ratios expressed herein are based on the amount of lipid in the composition, and not on the total amount of lipid in the composition. The ratio of immunogenic nucleic acid plasmid to lipids in a composition of the invention is suitably from about 1:1 to about 1:80 immunogenic nucleic acid plasmid:lipid by weight; from about 1:2 to about 1:40 immunogenic nucleic acid plasmid:lipid by weight; from about 1:3 to about 1:30 immunogenic nucleic acid:lipid by weight; or from about 1:6 to about 1:15 immunogenic nucleic acid plasmid:lipid by weight.

The concentration of the immunomodulatory composition, if elevated above a threshold, can be cytotoxic. For this reason, the concentration of the immunomodulatory composition as contemplated in the present disclosure is noncytotoxic, i.e., at a level below this threshold. “Cytotoxicity,” as used herein, refers to an abnormal cellular state such as failure to thrive, retarded growth, irregular microscopic appearance, and/or decline in immunoresponsiveness. In some aspects, the concentration of the immunomodulatory composition is between about 0.1 and about 250 ng/ml. In some aspects the concentration is between about 0.1 and about 200 ng/ml. In some aspects, the concentration of the immunomodulatory composition is between about 0.1 and about 150 ng/ml. In other aspects, the concentration of the immunomodulatory composition is between about 0.1 and about 100 ng/ml. In still other aspects, the concentration of the immunomodulatory complex is between about 0.1 and about 50 ng/ml. In other aspects, the concentration of the immunomodulatory composition is between about 1 and about 250 ng/ml. In some aspects, the concentration of the immunomodulatory composition is between about 10 and about 250 ng/ml. In some aspects, the concentration of the immunomodulatory composition is between about 50 and about 250 ng/ml. In some aspects, the concentration of the immunomodulatory composition is between about 100 and about 250 ng/ml. In some aspects, the concentration of the immunomodulatory composition is between about 150 and about 250 ng/ml. In still other aspects, the concentration of the immunomodulatory composition is between about 200 and about 250 ng/ml. In some embodiments, the concentration of the immunomodulatory composition is about or less than 120 ng/ml. In some aspects, the concentration of the immunomodulatory composition is non-cytotoxic.

Further provided herein are pharmaceutical compositions comprising an immunostimulatory composition as described supra and a pharmaceutically acceptable carrier. The immunomodulatory composition may be administered before, simultaneously with, or after immunostimulatory oligonucleotide. The pharmaceutical carriers for the individual immunomodulatory composition and immunostimulatory oligonucleotide may be but need not be the same carrier. The pharmaceutically acceptable carrier adapts the composition for administration by a route selected from intravenous, intramuscular, intramammary, intradermal, intraperitoneal, subcutaneous, by spray, by aerosol, in ovo, mucosal, transdermal, by immersion, oral, intraocular, intratracheal, intranasal, pulmonary, rectal, or other means known to those skilled in the art. The pharmaceutically acceptable carrier(s) may be a diluent, adjuvant, excipient, or vehicle with which the immunostimulatory composition is, or immunomodulatory composition and immunostimulatory oligonucleotide are, administered. Such vehicles may be liquids, such as water and oils, including those of petroleum, animal, vegetable, or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil, and the like. For example, 0.4% saline and 0.3% glycine can be used. These solutions are sterile and generally free of particulate matter. They may be sterilized by conventional, well-known sterilization techniques (e.g., filtration). The compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions such as pH adjusting and buffering agents, stabilizing, thickening, lubricating, and coloring agents, etc. The concentration of the molecules of the invention in such pharmaceutical formulation may vary widely, i.e., from less than about 0.5%, usually to at least about 1% to as much as 15 or 20% by weight and will be selected primarily based on required dose, fluid volumes, viscosities, etc., according to the particular mode of administration selected. Suitable vehicles and formulations, inclusive of other human proteins, e.g., human serum albumin, are described, for example, in e.g. Remington: The Science and Practice of Pharmacy, 21^(st) Edition, Troy, D. B. ed., Lipincott Williams and Wilkins, Philadelphia, Pa. 2006, Part 5, Pharmaceutical Manufacturing pp 691-1092, (see especially pp. 958-989).

Methods are also provided herein for preparing the immunostimulatory composition, described supra, comprising combining the immunomodulator composition and the immunostimulatory oligonucleotide, to form the immunostimulatory composition; centrifuging the immunostimulatory composition to generate a supernatant and a pellet; and isolating the pellet.

Centrifuging the immunostimulatory composition will cause the sedimentation of the immunostimulatory composition. Isolating the pellet may be accomplished by pouring off the supernatant, pipetting off the supernatant, or removing the supernatant by other means so long as a portion of the pellet remains. It is to be expected that some pellet will be lost during the removal of the supernatant. Also, some immunostimulatory composition may remain in the supernatant even after centrifugation. In such a scenario, the supernatant may retain immunostimulatory properties. If immunostimulatory activity due to the presence of the immunostimulatory composition remains in the supernatant but it is desired to have nearly all of the immunostimulatory composition in the pellet, higher centrifugation speeds should be used. For example, if the supernatant contains immunostimulatory composition after centrifugation at 8,000 rpm, increasing the centrifugation to 14,000 rpm may bring down the remaining immunostimulatory composition.

Also provided herein are methods for stimulating toll-like receptor 21 (TLR21) comprising administering an immunostimulatory oligonucleotide and an immunomodulator composition, wherein the immunostimulatory oligonucleotide comprises at least one CpG motif and an guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide, and wherein the immunomodulator composition comprises a noncoding nucleic acid plasmid and a cationic lipid delivery vehicle.

The immunostimulatory oligonucleotide and the immunomodulator composition can be administered by a route selected from intravenous, intramuscular, intramammary, intradermal, intraperitoneal, subcutaneous, by spray, by aerosol, in ovo, mucosal, transdermal, by immersion, oral, intraocular, intratracheal, intranasal, pulmonary, rectal, or other means known to those skilled in the art. In some aspects, the immunomodulator composition and the immunostimulatory oligonucleotide are present in synergistically effective amounts. The administration of the immunostimulatory composition and the immunomodulator composition may be sequential or simultaneous.

The concentration of the immunomodulator composition can be cytotoxic when above 250 μg/ml, and this cytotoxicity can more than offset any immunostimulatory effect of the immunomodulator. In some aspects of the present disclosures, the concentration of the immunomodulator is about 200 μg/ml. With administration of the immunostimulatory oligonucleotide, cytotoxic levels are not observed at or below the 10 μM range. Even higher concentrations of the immunostimulatory oligonucleotide may be tolerated by the recipient. In some aspects of the present disclosure the concentration of the immunostimulatory oligonucleotide is between about 10 μM and 0.5 μM. In some aspects the concentration of the immunostimulatory oligonucleotide is about 2 μM, and in some aspects, the concentration of the immunomodulator composition is greater than the concentration of the immunostimulatory oligonucleotide. Because cytotoxicity is a limiting factor with administration of the immunomodulator composition, in some aspects, the immunomodulator composition is present in non-cytotoxic amounts.

In each aspect of the methods presented herein, the immunomodulator composition and the immunostimulatory oligonucleotide can be any embodiment or aspect as described supra.

Also provided are methods for eliciting an immune response in a subject comprising administering any embodiment of the immunostimulatory composition described herein. Other embodiments included in the present disclosure include methods for eliciting an immune response in a subject comprising administering the immunostimulatory oligonucleotide and the immunomodulator composition described herein.

EXAMPLES

The following examples are provided to further describe some of the embodiments disclosed herein. The examples are intended to illustrate, not to limit, the disclosed embodiments.

The immunomodulator composition used in the following examples was a composition comprising a cationic lipid (DOTIM and cholesterol) and non-coding DNA (pMB75.6) (SEQ ID NO:266). The cationic lipid components were [1-[2-[9-(Z)-octadeceno-yloxy]]-2-[8](Z)-heptadecenyl]-3-[hydroxyethyl]imidazolinium chloride (DOTIM) and a synthetic neutral lipid cholesterol, formulated to produce liposomes approximately 200 nm in diameter (see, U.S. Pat. No. 6,693,086). The non-coding DNA component was a 4292 base-pair non-coding DNA plasmid (pMB75.6) (SEQ ID NO:266) produced in E. coli, which, being negatively charged, associates with the positively-charged (cationic) liposomes (see, U.S. Pat. No. 6,693,086). In the examples, the term “immunostimulatory nucleic acid plasmid” refers to pMB75.6.

Example 1: Combining TLR21-Active Oligodeoxynucleotides with an Immunomodulator Composition

The activity of the immunomodulator composition on TLR21 was explored. Specifically, HEK293-NFκB-bsd-cTLR21 cells were seeded into 384 well plates at 10,000 cells/well in 45 μl growth medium. These cells were exposed to the oligonucleotide dissolved in growth medium and incubated at 37° for 3-4 days. 10 μl of culture supernatant per well was transferred to a 384 well plate and 90 μl of 50 mM NaHCO₃/Na₂CO₃, 2 mM MgCl₂, 5 mM para-nitrophenylphospate (pNP) pH 9.6 were added and reaction rates were determined by kinetic measurement of the temporal changes of the optical density at 405 nM (mOD405 nm/min).

The immunostimulatory nucleic acid plasmid alone proved to be inactive in the concentration range considered (2 μg/ml and lower), while liposomally formulated immunostimulatory nucleic acid plasmid (pDNA-F) showed a weak but clear signal with a bell-shaped curve, indicating its interaction with TLR21 (FIG. 2A). The TLR21-stimulatory activity was, however, several orders of magnitude lower compared to 5-Chol-GCGT3-TG4T (SEQ ID NO:1) (FIGS. 2A and 2B), an oligonucleotide ligand optimized for interacting with this receptor.

TABLE 2 ODN sequences Immunostimulatory SEQ ID oligonucleotide NO Sequence 5Chol-GCGT3-TG4T SEQ ID XTGGGGTTTTTTTTGCGTTTTTGC (ODN1) NO: 1 GTTTTTGCGTTTT X = 5′-Cholesteryl GCGT3-TG4T SEQ ID TGGGGTTTTTTTTGCGTTTTTGCG (ODN2) NO: 252 TTTTTGCGTTTT 2006-PTO (ODN3) SEQ ID tcgtcgttttgtcgttttgtcgtt NO: 3

The activity of the immunomodulator composition pDNA-F on TLR21 suggests that this receptor may indeed be a component of the in vivo action of the immunomodulator composition, but because the immunomodulator composition is a rather weak ligand for TLR21, this receptor may not be the sole and dominant cognate receptor.

Example 2: Combination of 5-Chol-GCGT3-TG4T with the Immunostimulatory Nucleic Acid Plasmid and the Immunomodulator Composition

200 μg/ml solutions of the immunostimulatory nucleic acid plasmid alone and the immunomodulator composition and 2 μM solutions of 5-Chol-GCGT3-TG4T were prepared and incubated for 2 h at 4° C. Subsequently, from this solution, serial 1:2 dilutions were prepared and administered to HEK293-bsd-cTLR21 cells starting at 20 nM plasmid concentration (and 2 μg/ml plasmid concentration) according to the protocol in Example 1 and compared to a sample containing only 5-Chol-GCGT3-TG4T. All samples showed strong TLR21 stimulatory activity, with the only sample showing slightly higher peak values and an EC₅₀ of 2.44 pM (FIG. 3A, Table 3). Except for showing a slightly lower V_(max), combination of 5-Chol-GCGT3-TG4T with the immunostimulatory nucleic acid plasmid, which by itself was totally inactive, led to little change in EC₅₀, compared to 5-Chol-GCGT3-TG4T alone (2.11 pM) (FIG. 3A, Table 3). By contrast, the liposome-containing sample (immunostimulatory oligonucleotide 5-Chol-GCGT3-TG4T and the immunomodulator composition) showed an activity maximum and a strong signal decrease at higher concentrations, (FIG. 3A). However, closer inspection of low concentrations (pM) revealed a defined activity plateau with a calculated EC₅₀ of 1.04 pM (FIG. 3B, Table 3). In this concentration range, the immunomodulator composition is also totally inactive (FIG. 3B) and is, by itself, not responsible for the lower EC₅₀.

TABLE 3 Half-maximum effective concentration (EC₅₀) and maximum signal velocity (V_(max)) Vmax milliOD 405 nm/min Immunostimulant EC₅₀ (pM) (mOD405/min) 5-Chol-GCGT3-TG4T 2.44 338 5-Chol-GCGT3-TG4T- 2.11 260 pDNA combination 5-Chol-GCGT3-TG4T- 1.04 254 pDNA-F combination

The results suggest that the combination of the TLR21-stimulatory ODN 5-Chol-GCGT3-TG4T and non-cytotoxic concentrations of either immunostimulatory nucleic acid plasmid or the immunomodulator composition leads to active mixtures. Furthermore, the combination of the TLR21-stimulatory ODN 5-Chol-GCGT3-TG4T and the immunomodulator composition is synergistic with respect to the EC₅₀ of TLR21 activation.

Example 3: Centrifugation of the Immunomodulator Composition and TLR21 Activity

An immunomodulator composition solution of 200n/m1 plasmid concentration was centrifuged for 2 hours at 4° C. in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. For comparison, a non-centrifuged aliquot was stored at 4° C. for 2 hours. The supernatant was removed and stored, while the pellet was resuspended in an equivalent volume. Titrations starting at a 2 mg/ml plasmid content were prepared for use in the TLR21 assay as described in Example 1, as it had been established earlier that the immunomodulator composition possesses some weak TLR21 stimulatory activity (see Example 1).

Centrifugation of the immunomodulator composition resulted in a pellet that was difficult to resuspend with a pipette. All TLR21 stimulatory activity of immunomodulator composition was found in the pellet after centrifugation, and the supernatant was devoid of TLR21 activity (FIG. 4 ). The resuspended liposomes exhibited higher EC₅₀'s for TLR21 stimulation compared to the liposomes stored at 4° C. This effect may be due to changes in the liposomes after centrifugation (e.g., incomplete resuspension/dispersion).

Example 4: Combination of 5-Chol-GCGT3-TG4T with Immunomodulator Composition

An immunomodulator composition/5-Chol-GCGT3-TG4T solution having a 200 μg/ml plasmid concentration and 2 μM 5-Chol-GCGT3-TG4T was prepared. A 2 μM solution of 5-Chol-GCGT3-TG4T was also prepared. Both samples were incubated for 2 hours at 4° C. 100 μl aliquots of these solutions were centrifuged in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. for 2 hours for use in Example 5, while the remainder of the incubations were stored at 4° C. for analysis according to this Example 4. Both samples showed potent TLR21 stimulatory activity, but the immunomodulator composition/5-Chol-GCGT3-TG4T combination showed strongly decreasing signals at higher concentrations (FIG. 5A), likely a consequence of immunomodulator composition cytotoxicity. The respective V_(max) values were similar when the immunomodulator composition component of the sample was considered at low toxicity concentrations (FIG. 5B, Table 4). However, the calculated EC₅₀ of the combination immunomodulator composition/5-Chol-GCGT3-TG4T was 4-fold lower than that of 5-Chol-GCGT3-TG4T alone (FIG. 5B, Table 4).

TABLE 4 Half-maximum effective concentration (EC₅₀) and maximum signal velocity (V_(max)) Vmax milliOD 405 nm/min Immunostimulant EC₅₀ (pM) (mOD405/min) 5-Chol-GCGT3-TG4T 3.2 158 5-Chol-GCGT3-TG4T 2.5 160 (centrifugation supernatant) 5-Chol-GCGT3-TG4T 819 184 (centrifugation pellet) 5-Chol-GCGT3-TG4T- 0.62 160 pDNA-F combination 5-Chol-GCGT3-TG4T- 5145 184 pDNA-F combination (centrifugation supernatant) 5-Chol-GCGT3-TG4T- 1.81 140 pDNA-F combination (centrifugation pellet)

Example 5: Centrifugation of Immunomodulator Composition/5-Chol-GCGT3-TG4T and 5-Chol-GCGT3-TG4T

An immunomodulator composition/5-Chol-GCGT3-TG4T solution having a 200 μg/ml plasmid concentration and 2 μM 5-Chol-GCGT3-TG4T was prepared. A 2 μM solution of 5-Chol-GCGT3-TG4T was also prepared. Both samples were incubated for 2 hours at 4° C. 100 μl aliquots of these solutions were centrifuged in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. for 2 hours. The supernatants were removed and stored, while the pellets were resuspended in 100 μl. Subsequently, from these solutions, serial 1:2 dilutions were prepared and administered to HEK293-bsd-cTLR21 cells starting at 20 nM plasmid concentration (and 2 μg/ml plasmid concentration) and compared to a sample containing only 5-Chol-GCGT3-TG4T.

Centrifugation of the immunomodulator composition/5-Chol-GCGT3-TG4T combination led to a clearly visible pellet, while no visible pellet was observed for 5-Chol-GCGT3-TG4T. The immunomodulator composition/5-Chol-GCGT3-TG4T combination pellet (“pDNA-F 5Chol Pellet”) was difficult to resuspend, but in the TLR21 assay as described in Example 1, it contained virtually all stimulating activity (FIGS. 6A and 6B), with only traces being detected in the supernatant (“pDNA-F 5Chol Uberstand”) (FIG. 6B, Table 4), albeit with higher EC₅₀ than the original sample (“pDNA-f F-Chol-GCGT3-TG4T”) (Table 4). This result suggests that after mixing with immunomodulator composition, 5-Chol-GCGT3-TG4T is quantitatively physically associated with the liposomal fraction. 5-Chol-GCGT3-TG4T alone, which, when centrifuged, remains almost exclusively (an estimated 99%, Table 4) in the supernatant, as expected from a soluble compound (FIGS. 7A and 7B).

Example 6: Combination of 5-Chol-GCGT3-TG4T and Immunomodulator Composition

An immunostimulatory composition with 200 μg/ml plasmid concentration and 2 μM 5-Chol-GCGT3-TG4T was prepared. A 2 μM solution of 5-Chol-GCGT3-TG4T was also prepared. Both samples were incubated for 2 hours at 4° C. 100 μl aliquots of these solutions were centrifuged in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. for 2 hours for use in Example 7, while the remainder of the incubations were stored at 4° C. for analysis according to this Example 6. The supernatants were removed and stored, while the pellets were resuspended in 200 Subsequently, from these solutions, serial 1:2 dilutions were performed and administered to HEK293-bsd-cTLR21 cells for TLR21 analysis according to the protocol in Example 1. The starting plasmid concentration was 20 nM (and 2 μg/ml plasmid concentration) and compared to a sample containing only 5-Chol-GCGT3-TG4T.

Both samples (“5-Chol-GCGT3-TG4T” and “pDNA-F/5-Chol-GCGT3-TG4T”) showed potent TLR21 stimulatory activity, but the immunomodulator composition/5-Chol-GCGT3-TG4T combination (“pDNA-F/5-Chol-GCGT3-TG4T”) showed strongly decreasing signals at higher concentrations (FIG. 8A), likely a consequence of immunomodulator composition cytotoxicity. The respective V_(max) values were very similar when the stimulatory activity of immunomodulator composition-containing sample was considered at low toxicity concentrations (FIG. 8B, Table 5). However, the calculated EC₅₀ of the combination immunomodulator composition/5-Chol-GCGT3-TG4T was 2-fold lower than that of 5-Chol-GCGT3-TG4T (“5-Chol-GCGT3-TG4T”) alone (FIG. 8B, Table 5).

TABLE 5 Half-maximum effective concentration (EC₅₀) and maximum signal velocity (V_(max)) Vmax milliOD EC₅₀ picomolar 405 nm/min Immunostimulant (pM) (mOD405/min) 5-Chol-GCGT3-TG4T 2.2 120 5-Chol-GCGT3-TG4T 2.7 153 (centrifugation supernatant) 5-Chol-GCGT3-TG4T 530 139 (centrifugation pellet) 5-Chol-GCGT3-TG4T- 0.94 113 pDNA-F combination 5-Chol-GCGT3-TG4T- 14983 224 pDNA-F combination (centrifugation supernatant) 5-Chol-GCGT3-TG4T- 8.96 116 pDNA-F combination (centrifugation pellet)

Example 7: Centrifugation of Immunomodulator Composition/5-Chol-GCGT3-TG4T and 5-Chol-GCGT3-TG4T

Centrifugation of the immunomodulator composition/5-Chol-GCGT3-TG4T combination led to a clearly visible pellet, while no visible pellet was observed for 5-Chol-GCGT3-TG4T. The immunomodulator composition/5-Chol-GCGT3-TG4T combination pellet was difficult to resuspend, but in a TLR21 assay as described in Example 1, it (“pDNA-F/5-Chol-GCGT3-TG4T pellet”) contained virtually all of the stimulating activity (FIG. 9B), albeit with higher EC₅₀ than the original sample (Table 5)), with only traces being detected in the supernatant (“pDNA-F/5-Chol-GCGT3-TG4T supernatant”) (FIG. 9B, Table 5). This result suggests that after mixing with immunomodulator composition, the 5-Chol-GCGT3-TG4T is physically associated with the liposomal fraction. Both fractions were compared to non-centrifuged immunomodulator composition/5-Chol-GCGT3-TG4T (“pDNA-F/5-Chol-GCGT3-TG4T”)

Example 8: Combination of 5-Chol-GCGT3-TG4T with Immunomodulator Composition

An immunomodulator composition solution of 200 μg/ml plasmid concentration and 2 μM 5-Chol-GCGT3-TG4T was prepared. A 2 μM 5-Chol-GCGT3-TG4T sample also was prepared. Both samples were incubated for 2 hours at 4° C. 100 μl aliquots of these solutions were centrifuged in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. for 2 hours for use in Example 9, while the remainder of the incubations were stored at 4° C. for analysis according to this Example 8. The supernatants were removed and stored, while the pellets were resuspended in 100 μl. Subsequently, from these solutions, serial 1:2 dilutions were prepared and administered to HEK293-bsd-cTLR21 cells according to the protocol of Example 1, starting at 20 nM plasmid concentration (and 2 μg/ml plasmid concentration) and compared to a sample containing only 5-Chol-GCGT3-TG4T.

Both samples showed potent TLR21 stimulatory activity, but the 5-Chol-GCGT3-TG4T/immunomodulator composition combination (“pDNA-F/5-Chol-GCGT3-TG4T”) showed strongly decreasing signals at higher concentrations (FIG. 10A), similar to that of the immunomodulator by itself (“pDNA-F”) and likely a consequence of immunomodulator composition cytotoxicity. The immunostimulatory oligonucleotide (“5-Chol-GCGT3-TG4T”) exhibited greater stimulatory activity at higher concentrations than did either sample containing the immunomodulator composition. The respective V_(max) values were very similar when the stimulatory activity of immunomodulator composition component of the sample was considered at low toxicity concentrations (FIG. 10B, Table 6). However, the calculated EC₅₀ of the combination immunomodulator composition/5-Chol-GCGT3-TG4T (“pDNA-F/5-Chol-GCGT3-TG4T”) was 4-fold lower than that of 5-Chol-GCGT3-TG4T alone (“5-Chol-GCGT3-TG4T”) (FIG. 10B, Table 6). The immunomodulator composition alone (“Bay 98-F”) showed only minimal activity whose additive effect could not explain the increased activity of immunomodulator composition/5-Chol-GCGT3-TG4T versus 5-Chol-GCGT3-TG4T alone.

TABLE 6 Half-maximum effective concentration (EC₅₀) and maximum signal velocity (V_(max)): Vmax milliOD EC₅₀ picomolar 405 nm/min Immunostimulant (pM) (mOD405/min) 5-Chol-GCGT3-TG4T 2.47 53 5-Chol-GCGT3-TG4T- 0.59 51 pDNA-F combination 5-Chol-GCGT3-TG4T- 22.0 47 pDNA-F combination (centrifugation supernatant) 5-Chol-GCGT3-TG4T- 1.06 47 pDNA-F combination (centrifugation pellet)

Example 9: Centrifugation of Immunomodulator Composition

Centrifugation of immunomodulator composition/5-Chol-GCGT3-TG4T combination led to a clearly visible pellet, while for 5-Chol-GCGT3-TG4T, no visible pellet was observed. The immunomodulator composition/5-Chol-GCGT3-TG4T combination pellet (“pDNA-F/5-Chol-GCGT3-TG4T Pellet”) was difficult to resuspend, but in a TLR21 assay as described in Example 1, it contained >95% of the stimulating activity (FIG. 11B), albeit with higher EC₅₀ than the original sample, with only a small fraction (<5%) being detected in the supernatant (“pDNA-F/5-Chol-GCGT3-TG4T Supernatant”) (FIG. 11B, Table 6) and only slightly less than the non-centrifuged sample at low immunomodulator composition concentrations (“pDNA-F/5-Chol-GCGT3-TG4T”). This result suggests that after mixing with immunomodulator composition, 5-Chol-GCGT3-TG4T is quantitatively physically associated with the liposomal fraction.

Example 10: Combination of GCGT3-TG4T with Immunomodulator Composition

An immunomodulator composition solution of 200 μg/ml plasmid concentration and 2 μM GCGT3-TG4T (SEQ ID NO:252; the same oligonucleotide sequence as 5-Chol-GCGT3-TG4T (SEQ ID NO:1) but without the cholesteryl modification) was prepared. Also, a 2 μM GCGT3-TG4T sample was prepared, and both samples were incubated for 2 hours at 4° C. 100 μl aliquots of these solutions were centrifuged in an Eppendorf tabletop centrifuge at 14,000 rpm at 4° C. for 2 hours for use in Example 11, while the remainder of the incubations were stored at 4° C. for analysis according to this Example 10. The supernatants were removed and stored, while the pellets were resuspended in 100 μl. Subsequently, from these solutions, serial 1:2 dilutions were prepared and administered to HEK293-bsd-cTLR21 cells according to the protocol in Example 1, starting at 20 nM plasmid concentration (and 2 μg/ml plasmid concentration) and compared to a sample containing only GCGT3-TG4T.

Both samples showed potent TLR21 stimulatory activity, but the GCGT3-TG4T/immunomodulator composition combination (“pDNA-F/5-Chol-GCGT3-TG4T”) showed strongly decreasing signals at higher concentrations (FIG. 12A), likely a consequence of immunomodulator composition cytotoxicity. The respective V_(max) values were very similar, when the stimulatory activity of immunomodulator composition component of the sample was considered at low toxicity concentrations (FIG. 12B, Table 7). However, the calculated EC₅₀ of the combination immunomodulator composition/GCGT3-TG4T was more than 4-fold lower than that of GCGT3-TG4T alone (Table 7). The immunomodulator composition alone (“pDNA-F”) showed only minimal activity whose additive effect could not explain the increased activity of immunomodulator composition/GCGT3-TG4T versus GCGT3-TG4T alone.

TABLE 7 Half-maximum effective concentration (EC₅₀) and maximum signal velocity (V_(max)) Vmax milliOD EC₅₀ picomolar 405 nm/min Immunostimulant (pM) (mOD405/min) GCGT3-TG4T 324 56 GCGT3-TG4T- 69.4 51 pDNA-F combination GCGT3-TG4T- 860 43 pDNA-F combination (centrifugation supernatant) GCGT3-TG4T- 252 36 pDNA-F combination (centrifugation pellet)

Example 11: Centrifugation of Immunomodulator Composition/GCGT3-TG4T

Centrifugation of the immunomodulator composition/GCGT3-TG4T combination led to a clearly visible pellet. The immunomodulator composition/GCGT3-TG4T combination pellet was difficult to resuspend, but in a TLR21 assay as described in Example 1 it (“pDNA-F/GCGT3-TG4T Pellet”) contained >3× more stimulating activity (FIG. 13B), albeit with higher EC₅₀ than the original sample (“pDNA-F/GCGT3-TG4T”) than the supernatant (“pDNA-F/GCGT3-TG4T Supernatant”) (FIG. 13B, Table 7). This result suggests that after mixing with immunomodulator composition, the GCGT3-TG4T is quantitatively physically associated with the liposomal fraction, although perhaps not as efficiently as the cholesteryl-derivatized 5-Chol-GCGT3-TG4T.

Those skilled in the art will appreciate that numerous changes and modifications can be made to the preferred embodiments of the invention and that such changes and modifications can be made without departing from the spirit of the invention. It is, therefore, intended that the appended claims cover all such equivalent variations as fall within the true spirit and scope of the invention.

The disclosures of each patent, patent application, and publication cited or described in this document are hereby incorporated herein by reference, in its entirety.

Example 12: In Vivo Study of Efficacy of Immune Stimulants in a Newcastle Disease Vaccination Model in Chickens

To determine the suitability and efficacy of ODN1, ODN2, and ODN3 as immune stimulants, each was tested in three different concentrations.

The following immune stimulants were investigated:

ODN1: (SEQ ID NO: 1) [CholTEG]-TGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT (“5Chol-GCGT3-TG4T”) ([CholTEG]= 5′-triethyleneglycol-linked cholesteryl modification), ODN2: (SEQ ID NO: 252) TGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT (“GCGT3-TG4T”), ODN3: (SEQ ID NO: 3) tcgtcgttttgtcgttttgtcgtt (“2006-PTO”).

Each immune stimulant was added to an oil emulsion containing a suboptimal concentration of an inactivated Newcastle disease virus (NDV) according to Table 9. For the preparaton of the suboptimal NDV vaccine, the NDV antigen batch was diluted 50 times in NDV-negative allantoic fluid (AF). The efficacies of ODN1, ODN2, and ODN3 in combination with a suboptimal dosage of a Newcastle disease vaccine were tested in SPF layer chickens (Leghorn). The serological response was measured and compared to the similar suboptimal NDV vaccine without the immune stimulant. The antibody titre was determined at different time points after vaccination to investigate whether the addition of the immune stimulants leads to an earlier immune response. To determine the most optimal dosage of the three ODNs, each was supplemented in three different doses of 100 ng, 1000 ng and 5000 ng to the suboptimal NDV vaccine, resulting in nine immune stimulant groups. Besides these nine immune stimulant groups, five control groups were incorporated in this study, consisting of a suboptimal NDV vaccine without immune stimulant group, the non-diluted NDV vaccine group, a negative control group (immune stimulants in combination with adjuvant) and two positive control groups with polyinosinic:polycytidylic acid (poly I:C) at two different concentrations (Table 8).

The following parameters were tested: health of the chickens (data not shown) and serology by the Haemagglutination inhibition (HI) assay.

TABLE 8 Study Design Test Article/Control Item Test Group Number (n) Subootimal NDV + ODN1 100 ng T01 10 Subootimal NDV + ODN1 1000 ng T02 10 Subootimal NDV + ODN1 5000 ng T03 10 Subootimal NDV + ODN2 100 ng T04 10 Subootimal NDV + ODN2 1000 ng T05 10 Subootimal NDV + ODN2 5000 ng T06 10 Subootimal NDV + ODN3 100 ng T07 10 Subootimal NDV + ODN3 1000 ng T08 10 Subootimal NDV + ODN3 5000 ng T09 10 Suboptimal NDV T10 10 Optimal NDV (non-diluted vaccine) T11 10 ODN1 5000 ng + Adjuvant*  T12a 3 ODN2 5000 ng + Adjuvant*  T12b 3 ODN3 5000 ng + Adjuvant*  T12c 3 Adjuvant alone (Stimune)*  T12d 1 Suboptimal NDV + 10 μg Poly I:C T13 9 Suboptimal NDV + 100 μg Poly I:C T14 9 *3 animals were allocated as control for each immune stimulant in combination with the adjuvant (Stimune). One animal received the adjuvant only. All animals arrived at 3 weeks old. All animals were vaccinated at 5 weeks old. All vaccinations were performed at day 0 by intramuscular injection. Blood sampling/serology was performed on days 0 (before vaccination), 7, 14, and 21. Clinical scoring of all animals was performed daily.

Chickens enrolled in treatment groups T01-T14 received the Test Article or Control Item according to the study design. In groups T13 and T14, nine instead of ten chickens per group were vaccinated due to the loss of two animals before the start of the study.

Chickens allocated to treatment groups T01, T02, T03, T04, T05, T06, T07, T08 and T09 were vaccinated with a suboptimal NDV suspension containing 1 of 3 different immune stimulants (ODNs), each in 3 different concentrations (100, 1000, 5000 ng/dose). For the preparation of the water in oil emulsions, the NDV antigen suspension and immune stimulant (water phase) were formulated together with the adjuvant Stimune (oil phase) at a ratio of 4:5 (Table 9).

TABLE 9 Preparation of Test Articles and Control Items Water Phase Total Oil Phase volume Add volume NDV Neg. Stimune water water phase batch AF 600 ng/μl phase to Stimune Stimune Total Group Name (μl) (μl) (μl) (ml) (ml) (ml) (ml) T01 ODN1 100  100 4896 4 5 4 5 9 ng T02 ODN1 1000 100 4862 38 5 4 5 9 ng T03 ODN1 5000 100 4712 188 5 4 5 9 ng T04 ODN2 100  100 4896 4 5 4 5 9 ng T05 ODN2 1000 100 4862 38 5 4 5 9 ng T06 ODN2 5000 100 4712 188 5 4 5 9 ng T07 ODN3 100  100 4896 4 5 4 5 9 ng T08 ODN3 1000 100 4862 38 5 4 5 9 ng T09 ODN3 5000 100 4712 188 5 4 5 9 ng T10 Suboptimal 100 4900 0 5 4 5 9 vaccine T11 Non diluted 5000 0 0 5 4 5 9 vaccine T12a ODN1 5000 — 2887 113 3 2 2.5 4.5 ng in Stimune T12b ODN2 5000 — 2887 113 3 2 2.5 4.5 ng in Stimune T12c ODN3 5000 — 2887 113 3 2 2.5 4.5 ng in Stimune T12d Dilution — 2887 113 3 0.8 1 1.8 buffer (PBS) in Stimune T13 PolyI:C 10  100 4877 23 5 4 5 9 μg T14 PolyI:C 100 100 4675 225 5 4 5 9 μg ODN Preparation to 600 ng/μl 100 μM ODN Dilution Buffer Volume Stock 600 (μl) (μl) ng/μl (μl) ODN1 GCGT3-TG4T-5Chol 204 196 400 (SEQ ID NO: 1, see Table 1) ODN2 GCGT3-TG4T (SEQ 216 184 400 ID NO: 252, see Table 1) ODN3 2006-PTO (SEQ ID 312 88 400 NO: 3, see Table 1) Poly I:C 10 μg/μl Lyophilized Physiological Salt Volume Stock 10 Powder (mg) Solution (ml) μg/μl (μl) Control Poly I:C (P0913) 10 1 1000 Lot #s: 116M4118V #16TK5011 10 min 50□, 60 min RT (re-annealing) storage at −20□

Chickens allocated to control group of T10 were vaccinated with a suboptimal NDV suspension without immune stimulant in adjuvant (Stimune) at a ratio of 4:5.

Chickens allocated to control group of T11 were vaccinated with a non-diluted NDV suspension without immune stimulant in adjuvant (Stimune) at a ratio of 4:5.

Chickens allocated to group T12 were vaccinated with immune stimulant 1 (3 chickens), immune stimulant 2 (3 chickens) and immune stimulant 3 (3 chickens) in adjuvant (Stimune) at a ratio of 4:5. One chicken was vaccinated with dilution buffer (proprietary) in adjuvant (Stimune).

Chickens allocated to control groups of T13 (n=9) and T14 (n=9) were vaccinated with a suboptimal NDV suspension of NDV in combination with Poly I:C in two concentrations (10,000 ng and 100 μg) in adjuvant (Stimune) at a ratio of 4:5.

Test Article or Control Item Administration

The inactivated NDV strain Ulster suspension stored at −70° C. was thawed and diluted 50 times in negative allantoic fluid to create the suboptimal vaccine dose. Immune stimulants were added according to the study design. The resulting water phases were mixed with Stimune in a ratio of 4:5 according to the vaccination preparation scheme shown in Table 9. During preparation, all vaccine ingredients with the exception of the Stimune adjuvant were placed in melting ice. The formulated vaccines were injected (0.5 ml, intramuscular) directly after preparation.

General health was monitored by an experienced bio-technician daily from day of arrival until the end of the study.

Serum Blood Sampling

Blood samples for serology were collected from all chickens on study days 0 (prior to vaccination), 7, 14 and 21. Blood samples were labelled with the study number, a unique sample identification and the date of collection. Depending on the amount of the drawn blood volume, sera were aliquoted in two aliquots of approximately 0.5 ml and stored at −20±5° C.

Haemagglutination Inhibition (HI) Assay

In brief, dilution series of sera were incubated with 8 HAU (haemagglutinating units) of NDV strain Ulster at room temperature for 60 minutes. The HAU were titrated before each assay. Thereafter, chicken erythrocytes were added and agglutination was scored after incubation at 4° C. for 45 minutes. A negative control serum and three positive control sera, with low, intermediate and high antibody titres were included in each assay.

The HI titre results were expressed as the reciprocal of the highest serum dilution completely inhibiting agglutination, which were logarithmically transformed to the final Log 2 titres.

Statistics

Logarithmically transformed HI results were summarized per animal (see Tables 62-65). Per treatment group, the mean and standard deviation of the antibody titres were calculated. The statistical analysis was performed with the non-parametric Mann-Whitney t-test.

Results

No clinical symptoms or adverse events related to the vaccination were observed in all groups, all chickens appeared healthy during the entire study period.

Two chickens, however were scored with minor injuries due to pecking behaviour, which started 6 days before the start of the study. On the day of vaccination these chickens were allocated to the Poly I:C groups T13 (#11658) and T14 (#11676). Recovery took place within one week after vaccination.

ODN1, GCGT3-TG4T-5Chol

The individual HI results expressed as Log 2 titres of the 100 ng, 1000 ng and 5000 ng ODN1 dose groups are indicated in Table 10. The mean HI titres and standard deviation of these groups are indicated in FIG. 14 (days 14 and 21 post vaccination (pv)) and FIG. 15 (all data) compared to the mean titres of the diluted NDV vaccine group.

The GCGT3-TG4T-5Chol groups showed significantly higher HI titres compared to the diluted NDV vaccine (mean HI titre: 4.8 Log 2/SD 1.0). At day 14 pv this was the case for all three doses; 100 ng: mean HI titre 6.2 Log 2/SD 1.4 (p=0.0214), 1000 ng: mean HI titre 6.9 Log 2/SD 1.1 (p=0.0003) and 5000 ng: mean HI 5.9 Log 2/SD 0.7 (p=0.0243).

At day 21 pv, however, no significant differences were observed for all concentrations; 100 ng: mean HI titre 6.9 Log 2/SD 0.8 (p=0.1995); 1000 ng: mean HI titre 7.3 Log 2/SD 0.9 (p=0.0527); and 5000 ng: mean HI 6.7 Log 2/SD 0.9 (p=0.4523) when comparing to the NDV vaccine; HI titre 6.2 Log 2/SD1.0. (FIG. 14 ), although the 1000 ng concentration is very close to significance.

TABLE 10 Results duplo HI HI 1 HI 2 HI 1 HI 2 HI 1 HI 2 HI 3 HI 1 HI 2 HI 3 group Treatment animal d0 d0 mean d7 d7 mean d14 d14 d14 mean d21 d21 d21 mean T01 GCGT3-TG4T-5Chol 11402 0 0 0 1 1 1 7 7 7 7.0 7 7 7 7.0 100 ng 11404 0 0 0 0 0 0 7 7 7 7.0 7 7 7 7.0 11406 0 0 0 0 0 0 3 4 4 3.7 6 6 6 6.0 11408 0 0 0 0 0 0 7 8 8 7.7 8 9 7 8.0 11410 0 0 0 0 0 0 5 6 6 5.7 7 7 7 7.0 11412 0 0 0 0 0 0 6 6 8 6.7 6 6 6 6.0 11414 0 0 0 0 0 0 5 5 6 5.3 7 7 6 6.7 11416 0 0 0 0 0 0 8 7 8 7.7 8 8 8 8.0 11418 0 0 0 0 0 0 5 4 4 4.3 6 6 6 6.0 11420 0 0 0 0 0 0 8 7 7 7.3 7 7 8 7.3 mean 0.0 0.1 6.2 6.9 SD 0.0 0.3 1.4 0.8 T02 GCGT3-TG4T-5Chol 11422 0 0 0 0 0 0 7 6 7 6.7 6 6 6 6.0 1000 ng 11424 0 0 0 0 0 0 8 7 7 7.3 9 7 8 8.0 11426 0 0 0 0 0 0 6 5 5 5.3 6 6 6 6.0 11428 0 0 0 0 0 0 7 7 7 7.0 7 7 7 7.0 11430 0 0 0 1 1 1 10 9 10 9.7 8 8 9 8.3 11432 0 0 0 0 0 0 7 6 7 6.7 7 7 7 7.0 11434 0 0 0 0 0 0 7 6 6 6.3 7 7 7 7.0 11436 0 0 0 0 0 0 7 6 7 6.7 8 7 9 8.0 11438 0 0 0 0 0 0 7 6 6 6.3 7 7 7 7.0 11440 0 0 0 0 0 0 7 7 7 7.0 8 8 9 8.3 mean 0.0 0.1 6.9 7.3 SD 0.0 0.3 1.1 0.9 T03 GCGT3-TG4T-5Chol 11442 0 0 0 0 0 0 6 6 7 6.3 7 7 8 7.3 5000 ng 11444 0 0 0 0 0 0 5 5 5 5.0 6 6 6 6.0 11446 0 0 0 0 0 0 5 4 5 4.7 5 5 6 5.3 11448 0 0 0 0 0 0 7 7 7 7.0 8 8 9 8.3 11450 0 0 0 0 0 0 6 5 5 5.3 6 6 7 6.3 11452 0 0 0 0 0 0 6 5 6 5.7 7 7 7 7.0 11454 0 0 0 0 0 0 7 6 6 6.3 7 6 7 6.7 11456 0 0 0 0 0 0 6 6 6 6.0 6 6 6 6.0 11458 0 0 0 0 0 0 6 5 6 5.7 6 6 7 6.3 11460 0 0 0 0 0 0 7 6 7 6.7 7 7 8 7.3 mean 0.0 0.0 5.9 6.7 SD 0.0 0.0 0.7 0.9

ODN2, GCGT3-TG4T

The individual HI results expressed as Log 2 titres of the 100 ng, 1000 ng and 5000 ng ODN1 dose groups are indicated in Table 11. The mean HI titres and standard deviation of these groups are indicated in FIG. 16 (days 14 and 21 pv) and FIG. 17 (all data) compared to the mean titres of the diluted NDV vaccine group.

The ODN2, GCGT3-TG4T groups showed significantly higher HI titres compared to the diluted NDV vaccine (mean HI titre: 4.8 Log 2/SD 1.0). This was the case at day 14 post vaccination for all three doses; 100 ng: mean HI titre 7.1 Log 2/SD 1.2 (p=0.0003), 1000 ng: mean HI titre 6.4 Log 2/SD 0.7 (p=0.0027) and 5000 ng: mean HI titre 6.1 Log 2/SD 1.1 (p=0.0236). At day 21 significant differences were only observed at the 100 ng dose with a mean HI titre of 7.6 Log 2/SD 0.8 (p=0.0083) when compared to the NDV vaccine (HI titre 6.2 Log 2/SD 1.0). The mean HI titres for the 1000 ng and 5000 ng were 7.1 Log₂/0.6 (p=0.0696) and 7.2 Log 2/SD 1.0 (p=0.0956) respectively (FIG. 16 ).

TABLE 11 T04 GCGT3-TG4T 11462 0 0 0 0 0 0 7 6 7 6.7 7 7 7 7.3 100 ng 11464 0 0 0 0 0 0 8 7 8 7.7 7 8 8 7.7 11466 0 0 0 0 0 0 7 6 6 6.3 8 8 7 7.7 11468 0 0 0 0 0 0 8 7 8 7.7 8 9 8 8.3 11710 0 0 0 0 0 0 7 6 7 6.7 7 7 7 7.0 11472 0 0 0 0 0 0 10 10 9 9.7 10 9 8 9.0 11474 0 0 0 0 0 0 7 6 6 6.3 7 7 7 7.0 11476 0 0 0 0 0 0 6 5 5 5.3 7 7 6 6.7 11478 0 0 0 0 0 0 8 6 6 6.7 7 7 7 7.0 11480 0 0 0 0 0 0 9 8 7 8.0 9 9 8 8.7 mean 0.0 0.0 7.1 7.6 SD 0.0 0.0 1.2 0.8 T05 GCGT3-TG4T 11482 0 0 0 0 0 0 6 6 6 6.0 7 7 7 7.0 1000 ng 11484 0 0 0 0 0 0 6 6 7 6.3 7 7 7 7.0 11486 0 0 0 0 0 0 6 6 6 6.0 7 7 7 7.0 11488 0 0 0 0 0 0 6 8 6 6.7 8 8 8 8.0 11490 0 0 0 0 0 0 5 5 5 5.0 6 6 6 6.0 11492 0 0 0 0 0 0 7 7 7 7.0 7 7 8 7.3 11494 0 0 0 0 0 0 7 7 7 7.0 7 7 7 7.0 11496 0 0 0 0 0 0 6 6 6 6.0 7 8 7 7.3 11498 0 0 0 0 0 0 8 7 7 7.3 9 7 8 8.0 11500 0 0 0 0 0 0 7 6 6 6.3 7 6 7 6.7 mean 0.0 0.0 6.4 7.1 SD 0.0 0.0 0.7 0.6 T06 GCGT3-TG4T 11502 0 0 0 0 0 0 8 7 7 7.3 10 8 9 9.0 5000 ng 11504 0 0 0 0 0 0 7 7 6 6.7 8 7 7 7.3 11506 0 0 0 0 0 0 7 6 6 6.3 7 6 7 6.7 11508 0 0 0 0 0 0 6 5 5 5.3 8 6 7 7.0 11510 0 0 0 0 0 0 8 7 7 7.3 9 8 8 8.3 11512 0 0 0 0 0 0 8 6 7 7.0 9 7 8 8.0 11514 0 0 0 0 0 0 5 5 5 5.0 6 6 7 6.3 11516 0 0 0 0 0 0 7 6 6 6.3 7 7 7 7.0 11518 0 0 0 0 0 0 6 5 5 5.3 7 6 8 7.0 11520 0 0 0 0 0 0 4 4 4 4.0 6 5 6 5.7 mean 0.0 0.0 6.1 7.2 SD 0.0 0.0 1.1 1.0

ODN3, 2006-PTO

The individual HI results expressed as Log 2 titres of the 100 ng, 1000 ng and 5000 ng ODN1 dose groups measured are indicated in Table 12. During the triplicate HI assay performance an outlier result was observed for animal 11570 on day 21, this was most likely caused by a pipetting error (not enough AF added) and therefore this result was omitted from the final analysis (highlighted in Table 12). Thus, for this animal and date the mean HI titre was based on the duplicate measurement.

The mean HI titres and standard deviation of these groups are indicated in FIG. 18 (days 14 and 21 pv) and FIG. 19 (all data) compared to the mean titres of the diluted NDV vaccine group.

The ODN3, 2006-PTO groups showed significantly higher HI titres compared to the diluted NDV vaccine (mean HI titre: 4.8 Log 2/SD 1.0). This was the case at day 14 post vaccination for two doses; 1000 ng: mean HI titre: 6.3 Log 2/SD 1.2 (p=0.0081) and 5000 ng: mean HI titre: 6.2 Log 2/SD 0.8 (p=0.0059). The mean HI titre of the 100 ng dose was 5.3 Log 2/SD 0.5 (p=0.2090). At day 21 pv significant differences were only measured at the 5000 ng: mean HI titre 7.3 Log 2/SD 0.6 (p=0.0296). No significant differences were observed at the 100 ng and 1000 ng doses, with mean HI titres of 6.6 Log 2/SD 0.5 (p=0.7183) and 6.8 Log 2/SD 1.1 (p=0.1685) respectively, when comparing to the NDV vaccine; HI titre 6.2 Log 2/SD 1.0 (FIG. 18 ).

TABLE 12 T07 2006-PTO 11522 0 0 0 0 0 0 6 5 5 5.3 6 6 6 6.0 100 ng 11524 0 0 0 0 0 0 5 5 6 5.3 6 6 6 6.0 11526 0 0 0 0 0 0 6 5 6 5.7 7 7 7 7.0 11528 0 0 0 0 0 0 5 5 5 5.0 6 7 6 6.3 11530 0 0 0 0 0 0 6 5 7 6.0 7 7 7 7.0 11532 0 0 0 0 0 0 5 5 5 5.0 5 6 6 5.7 11534 0 0 0 0 0 0 5 5 6 5.3 7 7 7 7.0 11536 0 0 0 0 0 0 5 5 6 5.3 7 7 7 7.0 11538 0 0 0 0 0 0 4 4 5 4.3 7 6 7 6.7 11540 0 0 0 0 0 0 6 5 6 5.7 7 7 7 7.0 mean 0.0 0.0 5.3 6.6 SD 0.0 0.0 0.5 0.5 T08 2006-PTO 11542 0 0 0 0 0 0 6 5 6 5.7 6 6 7 6.3 1000 ng 11544 0 0 0 0 0 0 6 4 6 5.3 7 7 7 7.0 11546 0 0 0 0 0 0 4 4 5 4.3 4 5 4 4.3 11548 0 0 0 0 0 0 5 5 6 5.3 6 6 7 6.3 11550 0 0 0 0 0 0 7 7 7 7.0 7 7 8 7.3 11552 0 0 0 0 0 0 7 7 8 7.3 7 7 8 7.3 11554 0 0 0 0 0 0 8 8 9 8.3 8 8 9 8.3 11556 0 0 0 0 0 0 6 6 6 6.0 6 6 6 6.0 11558 0 0 0 0 0 0 7 7 7 7.0 7 7 8 7.3 11560 0 0 0 0 0 0 7 7 7 7.0 8 8 8 8.0 mean 0.0 0.0 6.3 6.8 SD 0.0 0.0 1.2 1.1 T09 2006-PTO 11562 0 0 0 0 0 0 6 6 6 6.0 7 7 8 7.3 5000 ng 11564 0 0 0 0 0 0 6 6 7 6.3 7 7 8 7.3 11566 0 0 0 0 0 0 6 6 7 6.3 7 7 7 7.0 11568 0 0 0 0 0 0 6 6 7 6.3 7 7 7 7.0 11570 0 0 0 0 0 0 5 5 6 5.3 7 11 7 7.0 11572 0 0 0 0 0 0 6 6 7 6.3 7 8 8 7.7 11574 0 0 0 0 0 0 5 5 6 5.3 6 7 7 6.7 11576 0 0 0 0 0 0 8 8 9 8.3 8 10 9 9.0 11578 0 0 0 0 0 0 6 6 7 6.3 7 7 7 7.0 11580 0 0 0 1 1 1 5 5 7 5.7 7 7 8 7.3 mean 0.0 0.1 6.2 7.3 SD 0.0 0.3 0.8 0.6

Control Groups

The individual HI results expressed as Log 2 titres of the 10 μg and 100 μg Poly I:C dose groups, the diluted and non-diluted NDV vaccines and the negative control groups are indicated in Table 13. The mean HI titres and standard deviation of these groups are indicated in FIG. 20 (days 14 and 21 pv) and FIG. 21 (all data) compared to the mean titres of the diluted NDV vaccine group.

For Poly I:C, the positive control groups, significantly higher HI titres were only observed at the 100 μg dose: HI titre 7.5 Log 2/SD 0.4 at day 21 (p=0.0053) when compared with the NDV vaccine (6.2 Log 2/SD 1.0). The mean HI titres at day 14 pv of the 10 μg and 100 μg dose groups were 5.8 Log 2/SD 1.3 (p=0.1859) and 5.5 Log 2/SD 0.8 (p=0.1609) respectively. The mean HI titre of the 10 μg dose group at day 21 pv was 6.4 Log 2/SD 1.3 (p=0.7273). Significant differences (p<0.0001) were observed between the non-diluted NDV vaccine (8.3/SD 0.5 and 8.5 Log 2/SD 0.7) and the negative control group compared to the diluted NDV group at days 14 and 21 post vaccination (4.8/SD 1.0 and 6.2 Log 2/SD 1.0, respectively) (FIG. 20 ).

TABLE 13 T10 Suboptimal vaccine 11582 0 0 0 0 0 0 4 4 4 4.0 6 5 6 5.7 (1:50) 11584 0 0 0 0 0 0 5 6 5 5.3 7 7 7 7.0 11586 0 0 0 0 0 0 5 5 6 5.3 5 5 6 5.3 11588 0 0 0 0 0 0 6 6 7 6.3 7 6 8 7.0 11590 0 0 0 0 0 0 4 4 5 4.3 6 6 6 6.0 11592 0 0 0 0 0 0 5 5 5 5.0 7 7 8 7.3 11594 0 0 0 0 0 0 4 4 5 4.3 6 7 8 7.0 11596 0 0 0 0 0 0 6 6 7 6.3 7 7 8 7.3 11598 0 0 0 0 0 0 4 4 4 4.0 4 4 5 4.3 11600 0 0 0 0 0 0 3 3 4 3.3 5 5 6 5.3 mean 0.0 0.0 4.8 6.2 SD 0.0 0.0 1.0 1.0 T11 Non diluted vaccine 11602 0 0 0 0 0 0 8 8 8 8.0 9 9 10 9.3 11604 0 0 0 0 0 0 9 9 8 8.7 8 9 10 9.0 11606 0 0 0 0 0 0 7 7 8 7.3 8 8 9 8.3 11608 0 0 0 0 0 0 8 9 9 8.7 9 9 10 9.3 11610 0 0 0 0 0 0 9 9 9 9.0 10 9 10 9.7 11612 0 0 0 0 0 0 8 8 9 8.3 8 8 8 8.0 11614 0 0 0 0 0 0 9 8 9 8.7 8 7 8 7.7 11616 0 0 0 0 0 0 8 8 8 8.0 7 8 8 7.7 11618 0 0 0 2 3 2.5 9 8 8 8.3 8 8 9 8.3 11620 0 0 0 0 0 0 8 8 8 8.0 8 8 8 8.0 mean 0.0 0.3 8.3 8.5 SD 0.0 0.8 0.5 0.7 T12 negative controles 11622 0 0 0 0 0 0 0 1 1 0.7 0 0 1 0.3 11624 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11626 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11628 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11630 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11632 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11634 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11636 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11638 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 11640 0 0 0 0 0 0 0 0 0 0.0 0 0 0 0.0 mean 0.0 0.0 0.1 0.0 SD 0.0 0.0 0.2 0.1 T13 Poly I:C 10 μg 11642 0 0 0 0 0 0 4 4 4 4.0 4 4 4 4.0 11644 0 0 0 0 0 0 6 6 6 6.0 7 7 7 7.0 11646 0 0 0 0 0 0 7 7 8 7.3 8 8 8 8.0 11648 0 0 0 0 0 0 5 4 5 4.7 6 6 6 6.0 11650 0 0 0 0 0 0 5 5 5 5.0 6 6 6 6.0 11652 0 0 0 0 0 0 7 7 7 7.0 7 7 7 7.0 11654 0 0 0 0 0 0 6 6 7 6.3 7 7 7 7.0 11656 0 0 0 0 0 0 4 4 4 4.0 5 5 5 5.0 11658 0 0 0 0 0 0 8 7 8 7.7 8 8 8 8.0 mean 0.0 0.1 5.8 6.4 SD 0.0 0.2 1.3 1.3 T14 Poly I:C 100 μg 11660 0 0 0 0 0 0 4 4 4 4.0 7 7 7 7.0 11662 0 0 0 0 0 0 4 4 5 4.3 7 7 7 7.0 11664 0 0 0 0 0 0 5 5 5 5.0 7 7 7 7.0 11666 0 0 0 0 0 0 6 6 6 6.0 7 7 8 7.3 11668 0 0 0 0 0 0 6 6 7 6.3 8 8 8 8.0 11670 0 0 0 0 0 0 6 6 6 6.0 7 8 8 7.3 11672 0 0 0 0 0 0 6 6 5 5.7 7 8 9 8.0 11674 0 0 0 0 0 0 6 6 5 5.7 8 8 8 8.0 11676 0 0 0 1 0 0.5 7 7 6 6.7 8 8 8 8.0 mean 0.0 0.1 5.5 7.5 SD 0.0 0.2 0.8 0.4

CONCLUSIONS

The goal was to study adjuvant activity of three different immune stimulants. This was tested by measuring the serological response after vaccination with oil emulsion vaccines containing a suboptimal concentration of inactivated NDV and different concentrations of one of three different immune stimulants.

The following immune stimulants were investigated:

ODN1: (SEQ ID NO: 1) [CholTEG]-TGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT (“GCGT3-TG4T-5Chol”) ([CholTEG] = 5′-triethyleneglycol-linked  cholesteryl modification), ODN2: (SEQ ID NO: 252) TGGGGTTTTTTTTGCGTTTTTGCGTTTTTGCGTTTT (“GCGT3-TG4T”), ODN3: (SEQ ID NO: 3) tcgtcgttttgtcgttttgtcgtt(“2006-PTO”).

The backbones of ODN1 and ODN2 immune were phosphodiester-linked, while the backbone of ODN3 was phosphorothioate-linked. The efficacy of each ODN was determined at three different doses; 100 ng, 1000 ng and 5000 ng, supplemented to the suboptimal NDV vaccine.

The serological response was determined at days 0 (prior to vaccination), 7, 14 and 21 after vaccination to investigate whether the addition of these immune stimulants may also lead to an earlier immune response. On days 0 and 7 post vaccination (pv) no antibody levels against NDV were detected, with the exception of one animal (#11618) in the non-diluted NDV vaccine group at day 7.

The serological response expressed as Log 2 HI titres showed significant differences (p<0.0001) between the non-diluted and the suboptimal NDV vaccines at days 14 and 21 pv, indicating that the dilution factor of 50 times was sufficient to create the suboptimal vaccine dose.

The negative control group remained negative during the entire study, indicating that the immune stimulants without NDV vaccine did not result in a non-specific immune response.

The positive control Poly I:C 100 μg dose group showed significantly higher HI titres compared to the naïve NDV vaccine at day 21 (p=0.0053), indicating that this dose group served as a valid positive control group.

The GCGT3-TG4T-5Chol (ODN1) group showed significantly higher HI titres when compared to the diluted NDV vaccine at day 14 pv for all three doses; 100 ng (p=0.0214), 1000 ng (p=0.0003) and 5000 ng (p=0.0243). At day 21 pv, however, no significant differences were observed.

The GCGT3-TG4T (ODN2) group showed significantly higher HI titres when compared to the diluted NDV vaccine at day 14 pv for all three doses; 100 ng (p=0.0003), 1000 ng (p=0.0027) and 5000 ng (p=0.0236). At day 21 significant differences (p=0.0083) were only measured at the 100 ng dose group.

The 2006-PTO (ODN3) group showed significantly higher HI titres compared to the diluted NDV vaccine at day 14 pv for two doses; 1000 ng (p=0.0081) and 5000 ng (p=0.0059). At day 21 pv significant differences (p=0.0296) were only measured at the 5000 ng dose group.

In conclusion, the highest mean HI titres were observed with the 100 ng GCGT3-TG4T (ODN2) dose group, 7.1 Log 2 (14 days pv) and 7.6 Log 2 (21 days pv), indicating an increase in titres when compared to the naïve NDV vaccine of 2.3 Log 2 and 1.4 Log 2 at day 14 and 21 pv, respectively.

The titres of the 1000 ng GCGT3-TG4T-5Chol (ODN1) dose group, 6.9 Log 2 and 7.3 Log 2, at day 14 and 21 pv respectively were almost similar to the ODN2 group. At day 14 pv no significant difference (p=0.7513) between ODN1 and ODN2 groups was observed.

The titres of the 5000 ng 2006-PTO (ODN3) dose group were 6.2 Log 2 and 7.3 Log 2 at day 14 and 21 pv, respectively. At day 14 pv, the ODN3 group significantly differed (p=0.0300) from both the ODN1 and ODN2 groups (FIG. 22 and FIG. 23 ).

At day 21 pv no significant differences between all ODN groups were shown.

These results therefore indicate that all ODNs were capable of significantly increasing the serological response, especially on day 14 after vaccination, also indicating an earlier onset of immunity. 

What is claimed:
 1. An immunostimulatory composition comprising: a) an immunomodulator composition comprising a nucleic acid plasmid and a liposomal delivery vehicle; and b) an immunostimulatory oligonucleotide having at least one CpG motif and a guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide.
 2. The immunostimulatory composition of claim 1, wherein the immunomodulator composition and the immunostimulatory oligonucleotide are present in synergistically effective amounts.
 3. The immunostimulatory composition of claim 1, wherein the immunostimulatory oligonucleotide comprises a ligand for a cytosolic nucleic acid surveillance molecule.
 4. The immunostimulatory composition of claim 3, wherein the immune cytosolic nucleic acid surveillance molecule is a toll-like receptor (TLR).
 5. The immunostimulatory composition of claim 3, wherein the cytosolic nucleic acid surveillance molecule is TLR21.
 6. The immunostimulatory composition of claim 1, wherein the nucleic acid plasmid concentration of the immunomodulator composition is greater than the concentration of the immunostimulatory oligonucleotide.
 7. The immunostimulatory composition of claim 1 further comprising a pharmaceutical carrier.
 8. The immunostimulatory composition of claim 1, wherein the liposomal delivery vehicle comprises multilamellar vesicle lipids, extruded lipids, or both.
 9. The immunostimulatory composition of claim 1, wherein the liposomal delivery vehicle is cationic.
 10. The immunostimulatory composition of claim 8, wherein the cationic liposomal delivery vehicle comprises pairs of lipids selected from the group consisting of N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTMA) and cholesterol; N-[1-(2,3-dioleoyloxy)propyl]-N,N,N-trimethylammonium chloride (DOTAP) and cholesterol; 1-[2-(oleoyloxy)ethyl]-2-oleyl-3-(2-hydroxyethyl)imidazolinium chloride (DOTIM) and cholesterol; and dimethyldioctadecylammonium bromide (DDAB) and cholesterol.
 11. The immunostimulatory composition of claim 1, wherein the nucleic acid plasmid is non-coding.
 12. The immunostimulatory composition of claim 1, wherein the nucleic acid plasmid has at least 75% sequence identity with SEQ ID NO.
 265. 13. The immunostimulatory composition of claim 1, wherein the nucleic acid plasmid has at least 75% sequence identity with SEQ ID NO.:266.
 14. The immunostimulatory composition of claim 1, wherein the nucleic acid plasmid has at least 75% sequence identity with SEQ ID NO:268.
 15. The immunostimulatory composition of claim 1, wherein the guanine nucleotide enriched sequence comprises a first plurality of guanine nucleotides.
 16. The immunostimulatory composition of claim 15, wherein the first plurality of guanine nucleotides comprises three to eight guanine nucleotides.
 17. The immunostimulatory composition of claim 15, wherein the immunostimulatory oligonucleotide comprises SEQ ID NO:16, 17, 18, 19, 20, 21, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 77, 78, 81, 82, 85, 86, 89, 90, 92, 93, 96, 97, 100, 102, 104, 106, 108, 143, or
 1. 18. The immunostimulatory composition of claim 15 further comprising a second plurality of guanine nucleotides downstream from the first plurality of guanine nucleotides.
 19. The immunostimulatory composition of claim 18, wherein the immunostimulatory oligonucleotide comprises SEQ ID NO:141, 142, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, or GCGT-Gwire3.
 20. The immunostimulatory compositions of claim 18 wherein the first plurality of guanine nucleotides and the second plurality of guanine nucleotides are separated by at least two nucleotides.
 21. The immunostimulatory compositions of claim 15, wherein the first plurality of guanine nucleotides and the at least one CpG motif is separated by at least 3 nucleotides.
 22. The immunostimulatory compositions of claim 15, wherein the first plurality of guanine nucleotides and the at least one CpG motif is separated by a hexaethyleneglycol, tetraethyleneglycol, propanediol, or derivatives thereof.
 23. The immunostimulatory composition of claim 22, wherein the structure of the hexaethyleneglycol is:


24. The immunostimulatory composition of claim 1, wherein the immunostimulatory oligonucleotide further comprises a plurality of CpG motifs, each CpG motif of the plurality of CpG motifs being separated from the others of the plurality of CpG motifs by a spacer.
 25. The immunostimulatory composition of claim 24, wherein the spacer comprises at least one nucleotide or nucleotide analog.
 26. The immunostimulatory composition of claim 25, wherein the spacer comprises a deoxyribosephosphate bridge.
 27. The immunostimulatory composition of claim 26, wherein the deoxyribosephosphate bridge is abasic.
 28. The immunostimulatory composition of claim 25, wherein the spacer comprises a carbon chain.
 29. The immunostimulatory composition of claim 28, wherein the carbon chain is derived from 1,3-propanediol.
 30. The immunostimulatory composition of claim 25, wherein the spacer comprises a repeated chemical unit.
 31. The immunostimulatory composition of claim 30, wherein the repeated chemical unit is an ethylene glycol.
 32. The immunostimulatory composition of claim 1, wherein the immunostimulatory oligonucleotide further comprises a phosphorothioate backbone.
 33. The immunostimulatory composition of claim 1, wherein the immunostimulatory oligonucleotide comprises a lipid moiety.
 34. The immunostimulatory composition of claim 33, wherein the lipid moiety is cholesteryl.
 35. The immunostimulatory composition of claim 33, wherein the lipid moiety is at or near the 5′ terminus of the immunostimulatory oligonucleotide.
 36. The immunostimulatory composition of claim 1, comprising a CpG sequence element at a 5′ terminus, a 3′ terminus, or both.
 37. The immunostimulatory composition of claim 36 having at least two CpG sequence elements.
 38. The immunostimulatory composition of claim 36, wherein the CpG sequence elements are GCGA, GCGG, ACGC, CCGC, GCGT, or TCGC.
 39. A method of preparing the immunostimulatory composition of claim 1 comprising: combining the immunomodulator composition and the immunostimulatory oligonucleotide, to form an immunostimulatory composition; centrifuging the immunostimulatory composition to generate a supernatant and a pellet; and isolating the pellet.
 40. A method for stimulating toll-like receptor 21 (TLR21) comprising: administering an immunostimulatory oligonucleotide and an immunomodulator composition, wherein the immunostimulatory oligonucleotide has at least one CpG motif and a guanine nucleotide enriched sequence at or near the 5′ terminus of the immunostimulatory oligonucleotide, and wherein the immunomodulator composition comprises a noncoding nucleic acid plasmid and a lipid delivery vehicle.
 41. The method of claim 40, wherein the immunomodulator composition and the immunostimulatory oligonucleotide are present in synergistically effective amounts.
 42. The method of claim 40, wherein the immunostimulatory oligonucleotide comprises a ligand for TLR21.
 43. A method of eliciting an immune response in a subject comprising administering to the subject the immunostimulatory composition of claim
 1. 44. An immunostimulatory composition comprising: a. a nucleic acid plasmid and a liposomal delivery vehicle; and b. an immunostimulatory oligonucleotide comprising SEQ ID NO:1.
 45. The immunostimulatory composition of claim 44, wherein the nucleic acid plasmid has at least 75% sequence identity with a sequence selected from the group consisting of SEQ ID NO:265, SEQ ID NO:266, SEQ ID NO:268.
 46. The immunostimulatory composition of claim 44, wherein the immunostimulatory oligonucleotide further comprises a 5′ cholesteryl modification.
 47. The immunostimulatory composition of claim 46, wherein the 5′ cholesteryl modification comprises a triethyleneglycol linker. 